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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameCORDIS STEERABLE PTCA BALLOON CATHETER
Classification Namecatheters, transluminal coronary angioplasty, percutaneous
Generic Nameptca catheter
Regulation Number870.5100
ApplicantCORDIS CORP.
PMA NumberP890032
Date Received01/31/1989
Decision Date03/06/1990
Withdrawal Date 09/02/2008
Product Code
LOX[ Registered Establishments with LOX ]
Docket Number 90M-0102
Notice Date 02/03/1990
Advisory Committee Cardiovascular
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S004 S006 S007 
S008 S009 S010 S011 S012 S013 
S014 S015 S016 S017 S018 S019 
S020 S021 S022 
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