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

SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER

K Number: K970823 · Decision Jun 3, 1997
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
109
Review Days
89

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Basic Information

Device Name
SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER
K Number
K970823
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
March 6, 1997
Decision Date
June 3, 1997
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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Other Clearances by Scimed Life Systems, Inc.

K Number Device Name
K974241 SCIMED INFORMER PRESSURE WIRE SYSTEM
K981788 SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETER
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
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
K964859 SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS
Search all 109 clearances from Scimed Life Systems, Inc. →