FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SCIMED TRIGUIDE GUIDE CATHETER

K Number: K944537 · Decision Oct 21, 1994
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
109
Review Days
36

Basic Information

Device Name
SCIMED TRIGUIDE GUIDE CATHETER
K Number
K944537
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SCIMED LIFE SYSTEMS, INC.
Date Received
September 15, 1994
Decision Date
October 21, 1994
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQY Catheter, Percutaneous

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K Number Device Name
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K980360 SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRES
K974559 SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS
K974684 SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER
K973945 LUGE GUIDE WIRE
K970823 SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER
K964551 CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID
K970244 SCIMED CHOICE FAMILY OF PTCA GUIDE WIRES
K965023 CHOICE PT PLUS PTCA GUIDE WIRE AND CHOICE PT VISION PTCA GUIDE WIRE
Search all 109 clearances from SCIMED LIFE SYSTEMS, INC. →