510(k) K791898 ยท HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered
OCUTOME MODEL 8000
| Applicant | Cooper Medical Devices Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 30, 1979 |
| Received | Sep 25, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791898
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.