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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameSTINGER, STINGER S, STINGER M, AND STINGER SM ABLATION CATHETER
Classification Namecardiac ablation percutaneous catheter
Generic Namecardiac ablation percutaneous catheter
ApplicantBoston Scientific Corp.
PMA NumberP000020
Supplement NumberS008
Date Received01/30/2003
Decision Date02/26/2003
Product Code
LPB[ Registered Establishments with LPB ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Change in the packaging for the bard stinger, stinger s, stinger m, and stinger sm ablation catheters.
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