510(k) K880929 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
NIDEK CV-4000
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, May 25, 1988 |
| Received | Mar 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880929
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.