FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

THE OPTIC BOX CONTACT LENS CASE

K Number: K895167 · Decision Jan 22, 1990
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
81
Applicant Total
1
Review Days
153

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Basic Information

Device Name
THE OPTIC BOX CONTACT LENS CASE
K Number
K895167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5928
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
The Optic Box Co., Ltd.
Date Received
August 22, 1989
Decision Date
January 22, 1990
Product Code
LRX
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
LRX Case, Contact Lens

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