510(k) K960374 ยท LFL Instrument, Ultrasonic Surgical
ULTRACUT 2000
| Applicant | Ultralase Technologies, Inc., Temple City CA, US |
| Decision | Substantially Equivalent, Jun 28, 1996 |
| Received | Jan 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960374
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.