510(k) K950056 ยท HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered
THE GRIESHABER AXIAL CUTTER
| Applicant | Grieshaber & Co., Kennesaw GA, US |
| Decision | Substantially Equivalent, May 5, 1995 |
| Received | Jan 6, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950056
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.