510(k) K950287 ยท HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered
UNIVIT PROBE
| Applicant | Medical Instrument Development Laboratories, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Apr 10, 1995 |
| Received | Jan 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950287
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.