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

BEMISS JASON-STERILE,NON-STERILE,REINFORCED STERILE,AND REINFORCED NON-STERILE SURGICAL GOWN

K Number: K962666 · Decision Feb 27, 1997
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
294
Applicant Total
1
Review Days
233

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Basic Information

Device Name
BEMISS JASON-STERILE,NON-STERILE,REINFORCED STERILE,AND REINFORCED NON-STERILE SURGICAL GOWN
K Number
K962666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bemiss-Jason Corp., Triad Medical Div.
Date Received
July 9, 1996
Decision Date
February 27, 1997
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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