510(k) K813389 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
ULTRASONIC FRAGMENTOR
| Applicant | Fibra Sonics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 4, 1982 |
| Received | Dec 3, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813389
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.