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

MERTEX-PLUS O.R./SURGEONS GOWN, NONSTERILE

K Number: K012240 · Decision Oct 15, 2001
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
294
Applicant Total
2
Review Days
90

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Basic Information

Device Name
MERTEX-PLUS O.R./SURGEONS GOWN, NONSTERILE
K Number
K012240
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mercan AB
Date Received
July 17, 2001
Decision Date
October 15, 2001
Product Code
FYA
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
FYA Gown, Surgical

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K Number Device Name
K012237 MERTEX-PLUS REUSABLE SURGICAL DRAPE