HER OPTION OFFICE CRYOABLATION THERAPY SYSTEM

Device, Thermal Ablation, Endometrial

FDA Premarket Approval P000032 S035

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Addition of a new manufacturing piece of equipment to assist in the production process.

DeviceHER OPTION OFFICE CRYOABLATION THERAPY SYSTEM
Classification NameDevice, Thermal Ablation, Endometrial
Generic NameDevice, Thermal Ablation, Endometrial
ApplicantCooperSurgical, Inc.
Date Received2010-01-26
Decision Date2010-02-25
PMAP000032
SupplementS035
Product CodeMNB
Advisory CommitteeObstetrics/Gynecology
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address CooperSurgical, Inc. 95 Corporate Dr. trumbull, CT 06611

Supplemental Filings

Supplement NumberDateSupplement Type
P000032Original Filing
S043 2017-12-12 Normal 180 Day Track
S042 2014-11-24 30-day Notice
S041 2013-06-17 30-day Notice
S040 2013-02-08 30-day Notice
S039 2013-02-08 30-day Notice
S038 2012-08-23 Normal 180 Day Track No User Fee
S037 2011-10-03 Normal 180 Day Track No User Fee
S036 2011-07-25 Normal 180 Day Track No User Fee
S035 2010-01-26 30-day Notice
S034 2010-01-25 30-day Notice
S033 2010-01-22 135 Review Track For 30-day Notice
S032 2010-01-21 135 Review Track For 30-day Notice
S031 2009-12-11 30-day Notice
S030 2009-11-23 Real-time Process
S029 2009-10-02 30-day Notice
S028 2008-06-06 Normal 180 Day Track
S027 2008-04-25 30-day Notice
S026 2008-03-18 30-day Notice
S025 2008-02-06 135 Review Track For 30-day Notice
S024 2008-01-09 30-day Notice
S023 2007-11-27 30-day Notice
S022 2007-10-17 135 Review Track For 30-day Notice
S021 2007-06-28 30-day Notice
S020 2006-05-17 135 Review Track For 30-day Notice
S019 2006-05-12 135 Review Track For 30-day Notice
S018 2006-03-31 135 Review Track For 30-day Notice
S017 2006-01-17 Special (immediate Track)
S016 2006-01-11 30-day Notice
S015
S014
S013 2005-08-13 Normal 180 Day Track
S012 2005-08-04 Real-time Process
S011 2005-06-09 30-day Notice
S010
S009 2005-05-02 30-day Notice
S008 2005-03-31 30-day Notice
S007
S006 2005-02-24 30-day Notice
S005 2004-01-20 Normal 180 Day Track No User Fee
S004 2003-12-08 Normal 180 Day Track No User Fee
S003 2003-04-24 Normal 180 Day Track No User Fee
S002
S001 2001-08-09 Special (immediate Track)

NIH GUDID Devices

Device IDPMASupp
20888937000027 P000032 000
00888937000016 P000032 000

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