510(k) K914221 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
KPE 220 TS, NONSTERILE
| Applicant | Ipax, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Oct 25, 1991 |
| Received | Aug 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914221
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.