510(k) K150271 ยท LFL Instrument, Ultrasonic Surgical
Prime Adaptive Ultrasonic Scalpel System
| Applicant | Endoprime, Inc., Blue Ash OH, US |
| Decision | Substantially Equivalent, May 29, 2015 |
| Received | Feb 4, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150271
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.