FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

VARIOUS CAMEO MED BASIC BIOPSY TRAYS, DISPOSABLE

K Number: K922962 · Decision Mar 23, 1993
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
3
Review Days
278

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Basic Information

Device Name
VARIOUS CAMEO MED BASIC BIOPSY TRAYS, DISPOSABLE
K Number
K922962
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Cameo, Inc.
Date Received
June 18, 1992
Decision Date
March 23, 1993
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, Antimicrobial

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KKX), ordered by most recent decision date.

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Other Clearances by Cameo, Inc.

K Number Device Name
K922961 VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,
K922960 VARIOUS CAMEO MED AMNIOCENTESIS TRAYS, DISPOSABLE