510(k) K031710 ยท LFL Instrument, Ultrasonic Surgical
OLYMPUS ULTRASONIC SURGICAL SYSTEM
| Applicant | Aomori Olympus Co., Ltd., Melville NY, US |
| Decision | Substantially Equivalent, Aug 29, 2003 |
| Received | Jun 2, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031710
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.