510(k) K890300 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE
| Applicant | CooperVision, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 17, 1989 |
| Received | Jan 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890300
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.