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

EYE PAD

K Number: K940333 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
16
Applicant Total
17
Review Days
41

Basic Information

Device Name
EYE PAD
K Number
K940333
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4440
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Certified Safety Mfg., Inc.
Date Received
January 25, 1994
Decision Date
March 7, 1994
Product Code
HMP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HMP Pad, Eye

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K945004 2, 3 & 4 BANDADGE COMPRESS
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K940249 CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING
K941311 FIRST AID/TRUMA KIT
K940358 X-LARGE MULTI-FUNCTION TRAUMA DRESSING
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