Certain Radiotherapy Systems and Treatment Planning Software, and Components Thereof; Institution of Investigation, 66934-66935 [2015-27668]
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Federal Register / Vol. 80, No. 210 / Friday, October 30, 2015 / Notices
personal identifying information in your
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your entire comment—including your
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be made publicly available at any time.
While you can ask us in your comment
to withhold your personal identifying
information from public review, we
cannot guarantee that we will be able to
do so.
Dated: September 21, 2015.
Jason Phillips,
Deputy Regional Director, Mid-Pacific Region.
[FR Doc. 2015–27716 Filed 10–29–15; 8:45 am]
BILLING CODE 4332–90–P
INTERNATIONAL TRADE
COMMISSION
[Inv. No. 337–TA–968]
Certain Radiotherapy Systems and
Treatment Planning Software, and
Components Thereof; Institution of
Investigation
U.S. International Trade
Commission.
ACTION: Notice.
AGENCY:
Notice is hereby given that a
complaint was filed with the U.S.
International Trade Commission on
September 25, 2015, under section 337
of the Tariff Act of 1930, as amended,
19 U.S.C. 1337, on behalf of Varian
Medical Systems, Inc. of Palo Alto,
California and Varian Medical Systems
International AG of Switzerland.
Supplements were filed on October 13,
2015. The complaint, as supplemented,
alleges violations of section 337 based
upon the importation into the United
States, the sale for importation, and the
sale within the United States after
importation of certain radiotherapy
systems and treatment planning
software, and components thereof by
reason of infringement of certain claims
of U.S. Patent No. 7,945,021 (‘‘the ’021
patent’’); U.S. Patent No. 8,116,430 (‘‘the
’430 patent’’); U.S. Patent No. 8,867,703
(‘‘the ’703 patent’’); U.S. Patent No.
7,880,154 (‘‘the ’154 patent’’); U.S.
Patent No. 7,906,770 (‘‘the ’770 patent’’);
and U.S. Patent No. 8,696,538 (‘‘the ’538
patent’’). The complaint further alleges
that an industry in the United States
exists as required by subsection (a)(2) of
section 337.
The complainants request that the
Commission institute an investigation
and, after the investigation, issue a
limited exclusion order and cease and
desist orders.
ADDRESSES: The complaint, except for
any confidential information contained
therein, is available for inspection
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:37 Oct 29, 2015
Jkt 238001
during official business hours (8:45 a.m.
to 5:15 p.m.) in the Office of the
Secretary, U.S. International Trade
Commission, 500 E Street SW., Room
112, Washington, DC 20436, telephone
(202) 205–2000. Hearing impaired
individuals are advised that information
on this matter can be obtained by
contacting the Commission’s TDD
terminal on (202) 205–1810. Persons
with mobility impairments who will
need special assistance in gaining access
to the Commission should contact the
Office of the Secretary at (202) 205–
2000. General information concerning
the Commission may also be obtained
by accessing its internet server at
https://www.usitc.gov. The public record
for this investigation may be viewed on
the Commission’s electronic docket
(EDIS) at https://edis.usitc.gov.
FOR FURTHER INFORMATION CONTACT: The
Office of Unfair Import Investigations,
U.S. International Trade Commission,
telephone (202) 205–2560.
Authority: The authority for institution of
this investigation is contained in section 337
of the Tariff Act of 1930, as amended, and
in section 210.10 of the Commission’s Rules
of Practice and Procedure, 19 CFR 210.10
(2015).
Scope of Investigation: Having
considered the complaint, the U.S.
International Trade Commission, on
October 26, 2015, ordered that—
(1) Pursuant to subsection (b) of
section 337 of the Tariff Act of 1930, as
amended, an investigation be instituted
to determine whether there is a
violation of subsection (a)(1)(B) of
section 337 in the importation into the
United States, the sale for importation,
or the sale within the United States after
importation of certain radiotherapy
systems and treatment planning
software, and components thereof by
reason of infringement of one or more of
claims 1, 2, 4–9, 11–16, 53–56, and 58–
62 of the ’021 patent; claims 1–4, 6–10,
12, 18, and 19 of the ’430 patent; claims
1–10, 12–15, and 17–21 of the ’703
patent; claims 19–28 and 33–36 of the
’154 patent; claims 61–63, 65, and 67–
70 of the ’770 patent; and claims 23, 25,
26, 39–42, 45, and 50 of the ’538 patent,
and whether an industry in the United
States exists as required by subsection
(a)(2) of section 337;
(2) Pursuant to Commission Rule
210.50(b)(1), 19 CFR 210.50(b)(1), the
presiding administrative law judge shall
take evidence or other information and
hear arguments from the parties and
other interested persons with respect to
the public interest in this investigation,
as appropriate, and provide the
Commission with findings of fact and a
recommended determination on this
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Fmt 4703
Sfmt 4703
issue, which shall be limited to the
statutory public interest factors set forth
in 19 U.S.C. 1337(d)(1), (f)(1), (g)(1);
(3) For the purpose of the
investigation so instituted, the following
are hereby named as parties upon which
this notice of investigation shall be
served:
(a) The complainants are:
Varian Medical Systems, Inc., 3100
Hansen Way, Palo Alto, CA 94304.
Varian Medical Systems International
AG, Hinterbergstrasse 14, 6330 Cham,
ZG, Switzerland.
(b) The respondents are the following
entities alleged to be in violation of
section 337, and are the parties upon
which the complaint is to be served:
Elekta AB, Kungstensgatan 18, SE–103
93 Stockholm, Sweden.
Elekta Ltd., Linac House, Fleming Way,
RH10 9RR Crawley, United Kingdom.
Elekta GmbH, Borsteler Chaussee 49,
22453 Hamburg, Germany.
Elekta Inc., 400 Perimeter Center
Terrace, Suite 50, Atlanta, GA 30346.
IMPAC Medical Systems, Inc., 100
Mathilda Place, 5th Floor, Sunnyvale,
CA 94086 .
Elekta Instrument (Shanghai) Limited,
Room 3202 & 3203, Pangu Plaza,
Office Building, Block A, No. 27
Fourth Ring Mid Road, Chaoyang
District, 100101 Shanghai, China.
Elekta Beijing Medical Systems Co. Ltd.,
No. 21, Chuang Xin Road, Science, &
Technology Park, Chang Ping, Beijing,
102200, China.
(c) The Office of Unfair Import
Investigations, U.S. International Trade
Commission, 500 E Street SW., Suite
401, Washington, DC 20436; and
(4) For the investigation so instituted,
the Chief Administrative Law Judge,
U.S. International Trade Commission,
shall designate the presiding
Administrative Law Judge.
Responses to the complaint and the
notice of investigation must be
submitted by the named respondents in
accordance with section 210.13 of the
Commission’s Rules of Practice and
Procedure, 19 CFR 210.13. Pursuant to
19 CFR 201.16(e) and 210.13(a), such
responses will be considered by the
Commission if received not later than 20
days after the date of service by the
Commission of the complaint and the
notice of investigation. Extensions of
time for submitting responses to the
complaint and the notice of
investigation will not be granted unless
good cause therefor is shown.
Failure of a respondent to file a timely
response to each allegation in the
complaint and in this notice may be
deemed to constitute a waiver of the
right to appear and contest the
E:\FR\FM\30OCN1.SGM
30OCN1
Federal Register / Vol. 80, No. 210 / Friday, October 30, 2015 / Notices
allegations of the complaint and this
notice, and to authorize the
administrative law judge and the
Commission, without further notice to
the respondent, to find the facts to be as
alleged in the complaint and this notice
and to enter an initial determination
and a final determination containing
such findings, and may result in the
issuance of an exclusion order or a cease
and desist order or both directed against
the respondent.
By order of the Commission.
Issued: October 26, 2015.
William R. Bishop,
Supervisory Hearings and Information
Officer.
[FR Doc. 2015–27668 Filed 10–29–15; 8:45 am]
BILLING CODE 7020–02–P
INTERNATIONAL TRADE
COMMISSION
[Investigation No. 731–TA–149 (Fourth
Review)]
Barium Chloride From China;
Determination
On the basis of the record 1 developed
in the subject five-year review, the
United States International Trade
Commission (‘‘Commission’’)
determines, pursuant to the Tariff Act of
1930, that revocation of the
antidumping duty order on barium
chloride from China would be likely to
lead to continuation or recurrence of
material injury to an industry in the
United States within a reasonably
foreseeable time.
tkelley on DSK3SPTVN1PROD with NOTICES
Background
The Commission, pursuant to section
751(c) of the Tariff Act of 1930 (19
U.S.C. 1675(c)), instituted this review
on May 1, 2015 (80 FR 24973) and
determined on August 4, 2015 that it
would conduct an expedited review (80
FR 50869, August 21, 2015).
The Commission made this
determination pursuant to section
751(c) of the Tariff Act of 1930 (19
U.S.C. 1675(c)). It completed and filed
its determination in this review on
October 27, 2015. The views of the
Commission are contained in USITC
Publication 4574 (October 2015),
entitled Barium Chloride from China:
Investigation No. 731–TA–149 (Fourth
Review).
By order of the Commission.
record is defined in sec. 207.2(f) of the
Commission’s Rules of Practice and Procedure (19
CFR 207.2(f)).
17:37 Oct 29, 2015
Jkt 238001
To submit
comments:
Send them to:
By mail .........
Assistant Attorney General,
U.S. DOJ—ENRD, P.O.
Box 7611, Washington, DC
20044–7611.
[FR Doc. 2015–27739 Filed 10–29–15; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Notice of Lodging of Proposed
Consent Decree Under the Clean Air
Act
On October 26, 2015, the Department
of Justice lodged a proposed Consent
Decree with the United States District
Court for the Northern District of Ohio
in the lawsuit entitled United States v.
Cleveland Thermal, LLC., Civil Action
No. 1:15–cv–2198.
In the Complaint, the United States
alleges that Cleveland Thermal, LLC,
(‘‘Cleveland Thermal’’) violated, at a
steam generating facility that it owns
and operates in Cleveland, Ohio, the
Prevention of Significant Deterioration
regulations, the Nonattainment New
Source Review regulations, and the
Standards of Performance for New
Stationary Sources, all promulgated
under the Clean Air Act, 42 U.S.C. 7401
et seq.
Under the Consent Decree, Cleveland
Thermal will retire all three of its coalfired boilers; will retire three of its five
fuel oil-fired boilers; and will operate its
remaining two fuel oil-fired boilers as
‘‘limited use’’ boilers. Cleveland
Thermal will install and operate new
natural gas-fired boilers to replace the
lost capacity. The new natural gas-fired
boilers must be properly permitted. In
addition, Cleveland Thermal may opt to
install and operate a properly permitted
new, natural gas-fired cogeneration
facility. Cleveland Thermal will pay a
civil penalty of $75,000 and perform an
environmental mitigation project worth
$350,000.
The publication of this notice opens
a period for public comment on the
Consent Decree. Comments should be
addressed to the Assistant Attorney
General, Environment and Natural
Resources Division, and should refer to
United States v. Cleveland Thermal,
LLC, D.J. Ref. No. 90–5–2–1–10579. All
comments must be submitted no later
than thirty (30) days after the
publication date of this notice.
Comments may be submitted either by
email or by mail:
To submit
comments:
1 The
VerDate Sep<11>2014
Issued: October 27, 2015.
William R. Bishop,
Supervisory Hearings and Information
Officer.
Send them to:
By e-mail ......
pubcomment-ees.enrd@
usdoj.gov.
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Fmt 4703
Sfmt 4703
66935
During the public comment period,
the Consent Decree may be examined
and downloaded at this Justice
Department Web site: https://
www.justice.gov/enrd/consent-decrees.
We will provide a paper copy of the
Consent Decree upon written request
and payment of reproduction costs.
Please mail your request and payment
to: Consent Decree Library, U.S. DOJ—
ENRD, P.O. Box 7611, Washington, DC
20044–7611
Please enclose a check or money order
for $24.75 (25 cents per page
reproduction cost) payable to the United
States Treasury. For a paper copy
without the exhibits and signature
pages, the cost is $15.50.
Randall M. Stone,
Acting Assistant Section Chief,
Environmental Enforcement Section,
Environment and Natural Resources Division.
[FR Doc. 2015–27615 Filed 10–29–15; 8:45 am]
BILLING CODE 4410–15–P
DEPARTMENT OF LABOR
Office of the Secretary
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; Resource
Justification Model
ACTION:
Notice.
The Department of Labor
(DOL) is submitting the Employment
and Training Administration (ETA)
sponsored information collection
request (ICR) revision titled, ‘‘Resource
Justification Model,’’ to the Office of
Management and Budget (OMB) for
review and approval for use in
accordance with the Paperwork
Reduction Act (PRA) of 1995 (44 U.S.C.
3501 et seq.). Public comments on the
ICR are invited.
DATES: The OMB will consider all
written comments that agency receives
on or before November 30, 2015.
ADDRESSES: A copy of this ICR with
applicable supporting documentation;
including a description of the likely
respondents, proposed frequency of
response, and estimated total burden
may be obtained free of charge from the
RegInfo.gov Web site at https://
www.reginfo.gov/public/do/
PRAViewICR?ref_nbr=201507-1205-002
SUMMARY:
E:\FR\FM\30OCN1.SGM
30OCN1
Agencies
[Federal Register Volume 80, Number 210 (Friday, October 30, 2015)]
[Notices]
[Pages 66934-66935]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-27668]
=======================================================================
-----------------------------------------------------------------------
INTERNATIONAL TRADE COMMISSION
[Inv. No. 337-TA-968]
Certain Radiotherapy Systems and Treatment Planning Software, and
Components Thereof; Institution of Investigation
AGENCY: U.S. International Trade Commission.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that a complaint was filed with the
U.S. International Trade Commission on September 25, 2015, under
section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, on
behalf of Varian Medical Systems, Inc. of Palo Alto, California and
Varian Medical Systems International AG of Switzerland. Supplements
were filed on October 13, 2015. The complaint, as supplemented, alleges
violations of section 337 based upon the importation into the United
States, the sale for importation, and the sale within the United States
after importation of certain radiotherapy systems and treatment
planning software, and components thereof by reason of infringement of
certain claims of U.S. Patent No. 7,945,021 (``the '021 patent''); U.S.
Patent No. 8,116,430 (``the '430 patent''); U.S. Patent No. 8,867,703
(``the '703 patent''); U.S. Patent No. 7,880,154 (``the '154 patent'');
U.S. Patent No. 7,906,770 (``the '770 patent''); and U.S. Patent No.
8,696,538 (``the '538 patent''). The complaint further alleges that an
industry in the United States exists as required by subsection (a)(2)
of section 337.
The complainants request that the Commission institute an
investigation and, after the investigation, issue a limited exclusion
order and cease and desist orders.
ADDRESSES: The complaint, except for any confidential information
contained therein, is available for inspection during official business
hours (8:45 a.m. to 5:15 p.m.) in the Office of the Secretary, U.S.
International Trade Commission, 500 E Street SW., Room 112, Washington,
DC 20436, telephone (202) 205-2000. Hearing impaired individuals are
advised that information on this matter can be obtained by contacting
the Commission's TDD terminal on (202) 205-1810. Persons with mobility
impairments who will need special assistance in gaining access to the
Commission should contact the Office of the Secretary at (202) 205-
2000. General information concerning the Commission may also be
obtained by accessing its internet server at https://www.usitc.gov. The
public record for this investigation may be viewed on the Commission's
electronic docket (EDIS) at https://edis.usitc.gov.
FOR FURTHER INFORMATION CONTACT: The Office of Unfair Import
Investigations, U.S. International Trade Commission, telephone (202)
205-2560.
Authority: The authority for institution of this investigation
is contained in section 337 of the Tariff Act of 1930, as amended,
and in section 210.10 of the Commission's Rules of Practice and
Procedure, 19 CFR 210.10 (2015).
Scope of Investigation: Having considered the complaint, the U.S.
International Trade Commission, on October 26, 2015, ordered that--
(1) Pursuant to subsection (b) of section 337 of the Tariff Act of
1930, as amended, an investigation be instituted to determine whether
there is a violation of subsection (a)(1)(B) of section 337 in the
importation into the United States, the sale for importation, or the
sale within the United States after importation of certain radiotherapy
systems and treatment planning software, and components thereof by
reason of infringement of one or more of claims 1, 2, 4-9, 11-16, 53-
56, and 58-62 of the '021 patent; claims 1-4, 6-10, 12, 18, and 19 of
the '430 patent; claims 1-10, 12-15, and 17-21 of the '703 patent;
claims 19-28 and 33-36 of the '154 patent; claims 61-63, 65, and 67-70
of the '770 patent; and claims 23, 25, 26, 39-42, 45, and 50 of the
'538 patent, and whether an industry in the United States exists as
required by subsection (a)(2) of section 337;
(2) Pursuant to Commission Rule 210.50(b)(1), 19 CFR 210.50(b)(1),
the presiding administrative law judge shall take evidence or other
information and hear arguments from the parties and other interested
persons with respect to the public interest in this investigation, as
appropriate, and provide the Commission with findings of fact and a
recommended determination on this issue, which shall be limited to the
statutory public interest factors set forth in 19 U.S.C. 1337(d)(1),
(f)(1), (g)(1);
(3) For the purpose of the investigation so instituted, the
following are hereby named as parties upon which this notice of
investigation shall be served:
(a) The complainants are:
Varian Medical Systems, Inc., 3100 Hansen Way, Palo Alto, CA 94304.
Varian Medical Systems International AG, Hinterbergstrasse 14, 6330
Cham, ZG, Switzerland.
(b) The respondents are the following entities alleged to be in
violation of section 337, and are the parties upon which the complaint
is to be served:
Elekta AB, Kungstensgatan 18, SE-103 93 Stockholm, Sweden.
Elekta Ltd., Linac House, Fleming Way, RH10 9RR Crawley, United
Kingdom.
Elekta GmbH, Borsteler Chaussee 49, 22453 Hamburg, Germany.
Elekta Inc., 400 Perimeter Center Terrace, Suite 50, Atlanta, GA 30346.
IMPAC Medical Systems, Inc., 100 Mathilda Place, 5th Floor, Sunnyvale,
CA 94086 .
Elekta Instrument (Shanghai) Limited, Room 3202 & 3203, Pangu Plaza,
Office Building, Block A, No. 27 Fourth Ring Mid Road, Chaoyang
District, 100101 Shanghai, China.
Elekta Beijing Medical Systems Co. Ltd., No. 21, Chuang Xin Road,
Science, & Technology Park, Chang Ping, Beijing, 102200, China.
(c) The Office of Unfair Import Investigations, U.S. International
Trade Commission, 500 E Street SW., Suite 401, Washington, DC 20436;
and
(4) For the investigation so instituted, the Chief Administrative
Law Judge, U.S. International Trade Commission, shall designate the
presiding Administrative Law Judge.
Responses to the complaint and the notice of investigation must be
submitted by the named respondents in accordance with section 210.13 of
the Commission's Rules of Practice and Procedure, 19 CFR 210.13.
Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be
considered by the Commission if received not later than 20 days after
the date of service by the Commission of the complaint and the notice
of investigation. Extensions of time for submitting responses to the
complaint and the notice of investigation will not be granted unless
good cause therefor is shown.
Failure of a respondent to file a timely response to each
allegation in the complaint and in this notice may be deemed to
constitute a waiver of the right to appear and contest the
[[Page 66935]]
allegations of the complaint and this notice, and to authorize the
administrative law judge and the Commission, without further notice to
the respondent, to find the facts to be as alleged in the complaint and
this notice and to enter an initial determination and a final
determination containing such findings, and may result in the issuance
of an exclusion order or a cease and desist order or both directed
against the respondent.
By order of the Commission.
Issued: October 26, 2015.
William R. Bishop,
Supervisory Hearings and Information Officer.
[FR Doc. 2015-27668 Filed 10-29-15; 8:45 am]
BILLING CODE 7020-02-P