510(k) K932669 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
SUPRA-VIT(TM)
| Applicant | Medical Instrument Development Laboratories, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Jun 3, 1994 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932669
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.