FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PROTEQ SURGEON'S GLOVES

K Number: K880632 · Decision Mar 31, 1988
Classifications
1
FEI Numbers
138
Registration Numbers
138
Same Product Code
558
Applicant Total
1
Review Days
44

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Basic Information

Device Name
PROTEQ SURGEON'S GLOVES
K Number
K880632
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4460
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Strategic Materials Group
Date Received
February 16, 1988
Decision Date
March 31, 1988
Product Code
KGO
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
KGO Surgeon'S Gloves

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