K903574 is an FDA 510(k) clearance for the CHIROFLEX LENS MICROSERT. This device is classified as a Lens, Guide, Intraocular (Class I - General Controls, product code KYB).
Submitted by Chiron Ophthalmics (Irvine, US). The FDA issued a Cleared decision on September 17, 1990, 40 days after receiving the submission on August 8, 1990.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4300.
| 510(k) Number | K903574 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 08, 1990 |
| Decision Date | September 17, 1990 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | KYB — Lens, Guide, Intraocular |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 886.4300 |