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

DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252

K Number: K931091 · Decision Feb 3, 1994
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
11
Review Days
337

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Basic Information

Device Name
DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252
K Number
K931091
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
Alliance Medical, Inc.
Date Received
March 3, 1993
Decision Date
February 3, 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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K Number Device Name
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K030187 REPROCESSED ELECTROPHYSIOLOGY CATHETER
K021654 REPROCESSED COMPRESSION SLEEVE
K012634 REPROCESSED EXTERNAL FIXATION DEVICE
K012630 REPROCESSED LINVATEC ARTHROSCOPIC BURS
K012611 REPROCESSED DYONICS ARTHROSCOPIC SHAVERS
K012613 REPROCSSED LINVATEC SHAVERS
K990198 AMIB7
K951976 ECHO. AKHO
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