510(k) K832074 ยท HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered
CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRA
| Applicant | CooperVision, Inc., Southampton, GB |
| Decision | Substantially Equivalent, Aug 1, 1983 |
| Received | Jun 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832074
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.