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

GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT

K Number: K941660 · Decision May 24, 1994
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
11
Review Days
49

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Basic Information

Device Name
GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT
K Number
K941660
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gm Engineering, Inc.
Date Received
April 5, 1994
Decision Date
May 24, 1994
Product Code
KYH
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
KYH Endoscope, Ophthalmic

Other Clearances by Gm Engineering, Inc.

K Number Device Name
K953348 ARTICULATING RETRACTOR TISSUE RETRACTORS
K942626 CONTINUOUS FLOW BIOPSY PROBE
K932394 BERNSTEIN(TM) UTERINE MANIPULATOR
K941661 GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT
K942703 GM REUSABLE AND DISPOSABLE TROCAR AND GM REUSABLE AND DISPOSABLE ULTRA-LIGHT CANNULA
K941662 GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHT
K933962 GM CONTINUOUS FLOW BIOPSY PROBE
K930611 TRUE FLOW(TM) VALVE
K934035 GM MONOPOLAR/FRAZIER SUCTION PROBE
K931398 GM SWIVEL VIDEO (TM) IRRIGATOR
Search all 11 clearances from Gm Engineering, Inc. →