510(k) K894248 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
CONVERTER SYSTEM
| Applicant | Mira, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Feb 27, 1990 |
| Received | Jun 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894248
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.