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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.
 
DeviceBETA-CATH(TM)SYSTEM
Generic NameIntravascular radiation delivery system
ApplicantBest Vascular, Inc.
4350 International Blvd.
Norcross, GA 30093
PMA NumberP000018
Supplement NumberS007
Date Received01/18/2001
Decision Date02/13/2001
Product Code MOU 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
CHANGE IN THE SUPPLIER AND THE MANUFACTURING METHOD USED IN FORMING THE PROPRIETARY CONNECTOR OF THE BETA-CATH(TM) DELIVERY CATHETER, FROM A MACHINED TO A MOLDED PROCESS.
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