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

WILLIAMS FLEXIBLE CYSTOSCOPIC INJECTION NEEDLE

K Number: K865086 · Decision Mar 10, 1987
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
52
Review Days
70

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
WILLIAMS FLEXIBLE CYSTOSCOPIC INJECTION NEEDLE
K Number
K865086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
December 30, 1986
Decision Date
March 10, 1987
Product Code
FBK
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FBK), ordered by most recent decision date.

View all

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. →