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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 NameE P TECH EPT-1000 CARDIAC ABLATION SYSTEM
Classification Namecardiac ablation percutaneous catheter
Generic Namecardiac ablation
ApplicantEP TECHNOLOGIES, INC.
PMA NumberP920047
Supplement NumberS007
Date Received02/11/1997
Decision Date06/24/1997
Product Code
LPB[ Registered Establishments with LPB ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason location change: manufacturer
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval to permit ept's manufacturing facility, located at 350 potrero ave. , sunnyvale, ca 94086, to be moved to a new facility at 2710 orchard parkway, san jose, ca.
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