510(k) K936302 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
NIDEK MODEL VT-4000, MODIFICATION
| Applicant | Nidek, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jul 15, 1994 |
| Received | Dec 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936302
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.