510(k) K940391 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE
| Applicant | Peregrine Surgical , Ltd., Doylestown PA, US |
| Decision | Substantially Equivalent, Jun 8, 1994 |
| Received | Jan 26, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940391
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.