K922253 is an FDA 510(k) clearance for the KERATOREF L60. This device is classified as a Keratoscope, Ac-powered (Class I - General Controls, product code HLQ).
Submitted by Luneau Ophtalmologie SA (Chartres Cedex, FR). The FDA issued a Cleared decision on June 19, 1992, 49 days after receiving the submission on May 1, 1992.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1350.
| 510(k) Number | K922253 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 01, 1992 |
| Decision Date | June 19, 1992 |
| Days to Decision | 49 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |
| Product Code | HLQ — Keratoscope, Ac-powered |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 886.1350 |