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

LipiView II Ocular Surface Interferometer

K Number: K152869 · Decision Jan 14, 2016
Classifications
1
FEI Numbers
67
Registration Numbers
68
Same Product Code
151
Applicant Total
7
Review Days
106

Basic Information

Device Name
LipiView II Ocular Surface Interferometer
K Number
K152869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TEARSCIENCE, INC.
Date Received
September 30, 2015
Decision Date
January 14, 2016
Product Code
HKI
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
HKI Camera, Ophthalmic, Ac-Powered

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