510(k) K961738 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
VIT COMMANDER SYSTEM
| Applicant | Scieran Technologies, Inc., Laguna Hills CA, US |
| Decision | Substantially Equivalent, Nov 25, 1996 |
| Received | May 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961738
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.