K896685 is an FDA 510(k) clearance for the BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM. This device is classified as a Case, Contact Lens (Class II - Special Controls, product code LRX).
Submitted by Bausch & Lomb, Inc. (Rochester, US). The FDA issued a Cleared decision on December 26, 1989, 28 days after receiving the submission on November 28, 1989.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5928.
| 510(k) Number | K896685 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 28, 1989 |
| Decision Date | December 26, 1989 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | - |
| Product Code | LRX - Case, Contact Lens |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.5928 |