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

SUN FILTERS/SHIELDS

K Number: K941829 · Decision May 17, 1994
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
1
Review Days
34

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Basic Information

Device Name
SUN FILTERS/SHIELDS
K Number
K941829
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4750
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Klinger Eye Shields, Inc.
Date Received
April 13, 1994
Decision Date
May 17, 1994
Product Code
HOY
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

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