510(k) K880166 ยท LFL Instrument, Ultrasonic Surgical
BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000
| Applicant | Clinical Technology Corp., Baltimore MD, US |
| Decision | Substantially Equivalent, Feb 18, 1988 |
| Received | Jan 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880166
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.