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

SURGICAL TOWEL

K Number: K902715 · Decision Sep 28, 1990
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
449
Applicant Total
1
Review Days
100

Basic Information

Device Name
SURGICAL TOWEL
K Number
K902715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
AZTEC MEDICAL, INC.
Date Received
June 20, 1990
Decision Date
September 28, 1990
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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