K091935 is an FDA 510(k) clearance for the LIPIVIEW OCULAR SURFACE INTERFEROMETER. This device is classified as a Camera, Ophthalmic, Ac-powered (Class II - Special Controls, product code HKI).
Submitted by Tearscience, Inc. (Morrisville, US). The FDA issued a Cleared decision on October 23, 2009, 115 days after receiving the submission on June 30, 2009.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1120.
| 510(k) Number | K091935 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 30, 2009 |
| Decision Date | October 23, 2009 |
| Days to Decision | 115 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | HKI — Camera, Ophthalmic, Ac-powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.1120 |