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

VAN-TEC BLADDER EVACUATOR

K Number: K880099 · Decision Mar 2, 1988
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
13
Applicant Total
52
Review Days
50

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Basic Information

Device Name
VAN-TEC BLADDER EVACUATOR
K Number
K880099
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4370
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
January 12, 1988
Decision Date
March 2, 1988
Product Code
KQT
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
KQT Evacuator, Gastro-Urology

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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
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
K870696 VAN-TEC SEGURA STONE BASKET W/PROTECTIVE SHEATH
Search all 52 clearances from Van-Tec, Inc. →