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

MAXIMUM CONTROL GOWN

K Number: K874318 · Decision Dec 2, 1987
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
67
Applicant Total
21
Review Days
43

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Basic Information

Device Name
MAXIMUM CONTROL GOWN
K Number
K874318
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ulti-Med Intl., Inc.
Date Received
October 20, 1987
Decision Date
December 2, 1987
Product Code
FYC
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
FYC Gown, Isolation, Surgical

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Other Clearances by Ulti-Med Intl., Inc.

K Number Device Name
K103011 ULTICARE SAFETY INSULIN SYRINGE
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K923175 SURGICAL INSTRUMENT KIT, DISPOSABLE
K920989 SURGICAL INSTRUMENT KIT, DISPOSABLE
K922828 ULCER WOUND TRAY
K914244 STERILE CUSTOM SURGICAL KITS
K914431 ABSORBENT FIBER
K912693 POST OPERATIVE SPONGE
K912692 CONFORMING BANDAGE
K904896 EYE PAD
Search all 21 clearances from Ulti-Med Intl., Inc. →