510(k) K801623 ยท LFL Instrument, Ultrasonic Surgical
CAVITRON ULTRASONIC SURG. ASPIR. CUSA
| Applicant | Cavitron Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 18, 1980 |
| Received | Jul 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801623
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.