K862517 is an FDA 510(k) clearance for the BAUSCH & LOMB CONTACT LENS VIEWER. This device is classified as a Device, Measuring, Lens Radius, Ophthalmic (Class I - General Controls, product code HLF).
Submitted by Bausch & Lomb, Inc. (Rochester, US). The FDA issued a Cleared decision on August 11, 1986, 41 days after receiving the submission on July 1, 1986.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1430.
| 510(k) Number | K862517 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 01, 1986 |
| Decision Date | August 11, 1986 |
| Days to Decision | 41 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | HLF — Device, Measuring, Lens Radius, Ophthalmic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 886.1430 |