510(k) K904909 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
I/A VITROPHAGE MODEL YPR 2001
| Applicant | Visioncare Devices, Inc., Redding CA, US |
| Decision | Substantially Equivalent, Jan 28, 1991 |
| Received | Oct 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904909
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.