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

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE

K Number: K925342 · Decision May 6, 1993
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
21
Review Days
198

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Basic Information

Device Name
MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE
K Number
K925342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronics Interventional Vascular
Date Received
October 20, 1992
Decision Date
May 6, 1993
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

Similar 510(k) Clearances

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Other Clearances by Medtronics Interventional Vascular

K Number Device Name
K990707 MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS
K980973 MEDTRONIC ANGIOGRAPHIC CATHETER
K982883 MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER
K981198 MEDTRONIC ZUMA GUIDING CATHETER
K972944 MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT
K961917 MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)
K960983 MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT
K955651 MEDTRONIC SHERPA GUIDING CATHETER
K950490 MEDTRONIC GC IV CORONARY GUIDING CATHETER
K950179 MEDTRONIC(R) GC III CORONARY GUIDING CATHETER
Search all 21 clearances from Medtronics Interventional Vascular →