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

SCIMED CHOICE PT VISION PTCA GUIDE WIRE

K Number: K962572 · Decision Dec 17, 1996
Classifications
1
FEI Numbers
252
Registration Numbers
253
Same Product Code
751
Applicant Total
109
Review Days
169

Basic Information

Device Name
SCIMED CHOICE PT VISION PTCA GUIDE WIRE
K Number
K962572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SCIMED LIFE SYSTEMS, INC.
Date Received
July 1, 1996
Decision Date
December 17, 1996
Product Code
DQX
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
DQX Wire, Guide, Catheter

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Other Clearances by SCIMED LIFE SYSTEMS, INC.

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. →