510(k) K822220 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
COOPER VISION I/A SYSTEM III MODEL 1500
| Applicant | CooperVision, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 6, 1982 |
| Received | Jul 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822220
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.