510(k) K912384 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
DISPOSABLE SUPPLIES KIT FOR PEA PROCEDURE
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Dec 24, 1991 |
| Received | May 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912384
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.