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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: 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.
 
DeviceObalon Balloon Kit, Obalon Navigation Balloon Kit, and Obalon Touch Balloon Kit
Generic NameIMPLANT, INTRAGASTRIC FOR MORBID OBESITY
ApplicantReShape Lifesciences, Inc.
1001 Calle Amanecer
San Clemente, CA 92673
PMA NumberP160001
Supplement NumberS041
Date Received06/03/2019
Decision Date07/03/2019
Product Code LTI 
Advisory Committee Gastroenterology/Urology
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Change a manufacturing fixture component and tighten a process set-up acceptance criterion relating to balloon welding.
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