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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.
 
DeviceVASOSEAL VHD & ES DEVICES
Generic NameDevice, hemostasis, vascular
ApplicantSt. Jude Medical, Inc.
177 E.COUNTY RD. B EAST
ST PAUL, MN 55117
PMA NumberP920004
Supplement NumberS016
Date Received02/05/2002
Decision Date03/07/2002
Withdrawal Date 12/06/2013
Product Code MGB 
Advisory Committee Cardiovascular
Supplement TypeSpecial (Immediate Track)
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR A CHANGE IN THE INSTRUCTIONS FOR USE. SPECIFICALLY, TO REMOVE THE OCCLUSIVE PRESSURE WHILE MAINTAINING ADHESIVE (DEVICE) PLUNGER PRESSURE AND POSITIONS AFTER THE FIRST COLLAGEN CARTRIDGE HAS BEEN DEPLOYED.
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