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

VANCE-AMBROSE RESECTOSCOPE FORCEPS

K Number: K812785 · Decision Nov 16, 1981
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
17
Review Days
42

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Basic Information

Device Name
VANCE-AMBROSE RESECTOSCOPE FORCEPS
K Number
K812785
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Vance Products, Inc.
Date Received
October 5, 1981
Decision Date
November 16, 1981
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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K812057 VANCE CYSTOSCOPIC
K811833 VNACE FASCIAL DILATOR SET
K811454 VANCE PROSTATIC ASPIRATION SET
K810367 KISH URETHRAL ILLUMINATED CATHETER SET
K810370 POLLACK CHAIN CYSOURETHROGRAM SET
K810368 VANCE PERCUTANEOUS MALECOT NEPHROSTOMY
K810372 VANCE DEFLECTABLE BIOPSY BRUSH SET
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