FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VAN-TEC ENDOPYELOTOMY KNIFE

K Number: K880094 · Decision Feb 29, 1988
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
20
Applicant Total
52
Review Days
48

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Basic Information

Device Name
VAN-TEC ENDOPYELOTOMY KNIFE
K Number
K880094
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
January 12, 1988
Decision Date
February 29, 1988
Product Code
EMF
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EMF Knife, Surgical

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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
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. →