510(k) K980399 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20
| Applicant | Peregrine Surgical , Ltd., Doylestown PA, US |
| Decision | Substantially Equivalent, Apr 30, 1998 |
| Received | Feb 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980399
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.