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

INSULATOR WIRE GUIDE

K Number: K972977 · Decision Oct 10, 1997
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
104
Review Days
60

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Basic Information

Device Name
INSULATOR WIRE GUIDE
K Number
K972977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Urological, Inc.
Date Received
August 11, 1997
Decision Date
October 10, 1997
Product Code
KNY
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNY Accessories, Catheter, G-U

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Other Clearances by Cook Urological, Inc.

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K082939 COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400
K082066 TAO BRUSH I.U.M.C. ENDOMETRIAL SAMPLER
K082536 COOK WIRE GUIDES
K082319 INJEKT FILIFORM INJECTION NEEDLE
K080525 COOK ODYSSEY HOLMIUM LASER SYSTEM, MODEL 30W
K073496 OPTILITE HOLMIUM LASER FIBERS
K072521 COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATH
K061371 SYDNEY IVF SPERM CRYOPRESERVATION BUFFER
Search all 104 clearances from Cook Urological, Inc. →