510(k) K970670 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
REUSABLE VITRECTOMY PROBE
| Applicant | Altex Vision, San Francisco CA, US |
| Decision | Substantially Equivalent, May 6, 1997 |
| Received | Feb 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970670
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.