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FDA 510(k) K122481, LIPIVIEW OCULAR SURFACE INTERFEROMETER, by Tearscience, Inc.

FDA 510(k) K122481, LIPIVIEW OCULAR SURFACE INTERFEROMETER, by Tearscience, Inc.

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510(K) Number: K122481
Device Name: LIPIVIEW OCULAR SURFACE INTERFEROMETER
Manufacturer: Tearscience, Inc.
Device Classification Name: camera, ophthalmic, ac-powered
Regulation Number: 886.1120
Classification Product Code: HKI
Date Received: 08/14/2012
Decision Date: 12/31/2012
Regulation Medical Specialty: Ophthalmic
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