LipiView II Ocular Surface Interferometer
K-Number: K152869 · 2016-01-14
ApplicantTearscience, Inc.
Decision Date2016-01-14
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
LipiView II Ocular Surface Interferometer is a medical device manufactured by Tearscience, Inc.. It received FDA 510(k) clearance on 2016-01-14 under approval number K152869. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LipiView II Ocular Surface Interferometer?
LipiView II Ocular Surface Interferometer is a medical device that received FDA 510(k) clearance on 2016-01-14. It is manufactured by Tearscience, Inc.. The 510(k) number is K152869.
When was LipiView II Ocular Surface Interferometer approved by the FDA?
LipiView II Ocular Surface Interferometer received FDA 510(k) clearance on 2016-01-14, under approval number K152869.
What company makes LipiView II Ocular Surface Interferometer?
LipiView II Ocular Surface Interferometer is manufactured by Tearscience, Inc..
What is the FDA product code for LipiView II Ocular Surface Interferometer?
The FDA product code for LipiView II Ocular Surface Interferometer is HKI.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.