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

FACE-IT SHIELD

K Number: K942022 · Decision Jul 8, 1994
Classifications
1
FEI Numbers
801
Registration Numbers
801
Same Product Code
55
Applicant Total
47
Review Days
73

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Basic Information

Device Name
FACE-IT SHIELD
K Number
K942022
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Onyx Medical Corp.
Date Received
April 26, 1994
Decision Date
July 8, 1994
Product Code
LYU
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
LYU Accessory, Surgical Apparel

Similar 510(k) Clearances

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Other Clearances by Onyx Medical Corp.

K Number Device Name
K931690 SPOON PLATE
K934614 MINI FRAGMENT PLATE
K931692 T-PLATE
K931684 EPIPHYSIS PLATE
K931680 CANNULATED CANCELLOUS SCREW
K931679 BUTTRESS PLATE
K934615 CANCELLOUS BONE SCREW
K931683 CLOVERLEAF PLATE
K931693 1/3 TUBULAR PLATE
K931687 MULTIPLE FRAGMENT PLATE
Search all 47 clearances from Onyx Medical Corp. →