510(k) K950799 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
PRO-VIT
| Applicant | M. Imonti and Associates Inc.,, San Juan Capistrano CA, US |
| Decision | Substantially Equivalent, Apr 28, 1995 |
| Received | Feb 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950799
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.