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

DEFLECTING GUIDE WIRE

K Number: K833242 · Decision Oct 19, 1983
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
52
Review Days
62

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Basic Information

Device Name
DEFLECTING GUIDE WIRE
K Number
K833242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
August 18, 1983
Decision Date
October 19, 1983
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 Van-Tec, Inc.

K Number Device Name
K880098 VAN-TEC AUTO BIOPSY NEEDLE
K880096 VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUP
K880095 BERGER PROSTATE CULTURE CYTOLOGY BRUSH
K880099 VAN-TEC BLADDER EVACUATOR
K880094 VAN-TEC ENDOPYELOTOMY KNIFE
K874112 VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER
K871777 VAN-TEC REUSABLE HELICAL STONE BASKET
K871779 HELICAL STONE BASKET (DISPOSABLE)
K870679 VAN-TEC MODULAR FLEXIBLE CYSTOURETHROSCOPE
K870557 VAN-TEC PUMPING SYSTEM
Search all 52 clearances from Van-Tec, Inc. →