510(k) K833371 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
DISPOSABLE OCUTOME PROBE
| Applicant | CooperVision, Inc., Southampton, GB |
| Decision | Substantially Equivalent, Jan 4, 1984 |
| Received | Sep 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833371
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.