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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.
 
DeviceFalope Ring Bands
Generic NameLaparoscopic contraceptive tubal occlusion device
Regulation Number884.5380
ApplicantGyrus ACMI, Inc.
136 TURNPIKE RD.
SOUTHBOROUGH, MA 01772
PMA NumberP870076
Supplement NumberS025
Date Received04/03/2020
Decision Date07/02/2020
Product Code KNH 
Advisory Committee Obstetrics/Gynecology
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Falope-Ring Band (FRB-30) sterilization site change from Viant to Steris, Inc. in Minneapolis, Minneapolis.
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