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

SURGICAL DRAPES

K Number: K943122 · Decision Sep 7, 1994
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
27
Review Days
70

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Basic Information

Device Name
SURGICAL DRAPES
K Number
K943122
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mallinckrodt Group, Inc.
Date Received
June 29, 1994
Decision Date
September 7, 1994
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

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K905789 FRANKLIN 9000 WALL STAND
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