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FDA 510(k), K091935, LIPIVIEW OCULAR SURFACE INTERFEROMETER
FDA 510(k), K091935, LIPIVIEW OCULAR SURFACE INTERFEROMETER
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510(K) Number: K091935
Device Name: LIPIVIEW OCULAR SURFACE INTERFEROMETER
Manufacturer: CHRISTY STEVENS
Device Classification Name: Camera, Ophthalmic, Ac-Powered
Regulation Number: HKI
Classification Product Code: KXA
Date Received: 06/30/2009
Decision Date: 10/23/2009
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
Device Name: LIPIVIEW OCULAR SURFACE INTERFEROMETER
Manufacturer: CHRISTY STEVENS
Device Classification Name: Camera, Ophthalmic, Ac-Powered
Regulation Number: HKI
Classification Product Code: KXA
Date Received: 06/30/2009
Decision Date: 10/23/2009
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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