LEOCOR CORFLO(TM) MODEL 7.5PT & PICO-ST COATED CAT

FDA Premarket Approval P890001 S012

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.

Pre-market Approval Supplement Details

DeviceLEOCOR CORFLO(TM) MODEL 7.5PT & PICO-ST COATED CAT
Generic NameCatheters, Transluminal Coronary Angioplasty, Percutaneous
ApplicantLEOCOR, INC.
Date Received1995-03-03
Decision Date1995-04-27
PMAP890001
SupplementS012
Product CodeLOX 
Advisory CommitteeCardiovascular
Supplement Type30-Day Supplement
Supplement ReasonLabeling Change - Indications/instructions/shelf Life/tradename
Expedited ReviewNo
Combination Product No
Applicant Address LEOCOR, INC. 1301 Regents Pk. Dr. houston, TX 77058

Supplemental Filings

Supplement NumberDateSupplement Type
P890001Original Filing
S020 1996-11-29 Normal 180 Day Track
S019 1996-10-03 Normal 180 Day Track
S018 1996-09-09 Normal 180 Day Track
S017
S016 1996-04-18 Normal 180 Day Track
S015 1995-12-01 Normal 180 Day Track
S014 1995-06-21 30-Day Supplement
S013
S012 1995-03-03 30-Day Supplement
S011 1994-09-01 Normal 180 Day Track
S010 1993-10-07 Normal 180 Day Track
S009 1993-09-16 Normal 180 Day Track
S008
S007 1991-12-23 Normal 180 Day Track
S006 1991-09-27 Normal 180 Day Track
S005 1991-05-14 Normal 180 Day Track
S004 1990-10-15 Normal 180 Day Track
S003 1990-02-14 Normal 180 Day Track
S002 1990-05-17 Panel Track
S001 1990-04-10 Normal 180 Day Track

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