510(k) K922996 ยท KYG Device, Irrigation, Ocular Surgery
MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS
| Applicant | Chiron Vision Corp., Horsham PA, US |
| Decision | Substantially Equivalent, Jul 27, 1992 |
| Received | Jun 22, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922996
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.