510(k) K002906 ยท LFL Instrument, Ultrasonic Surgical
ULTRACISION HARMONIC SCALPEL SYSTEM, MODELS GEN01, GEN02, GEN03, HP052, HP053, HSA07
| Applicant | Ethicon Endo-Surgery, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Dec 15, 2000 |
| Received | Sep 18, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002906
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.