510(k) K992943 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
VIT ENHANCER
| Applicant | Medical Instrument Development Laboratories, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Dec 10, 1999 |
| Received | Aug 31, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992943
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.