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

DRAPE, MICROSCOPE

K Number: K792176 · Decision Dec 10, 1979
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
449
Applicant Total
1
Review Days
40

Basic Information

Device Name
DRAPE, MICROSCOPE
K Number
K792176
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
CHRIS CO., INC.
Date Received
October 31, 1979
Decision Date
December 10, 1979
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical

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