510(k) K143562 ยท NLQ Single-Use Reprocessed Ultrasonic Surgical Instruments
Reprocessed Cordless Ultrasonic Dissection Device
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, May 20, 2015 |
| Received | Dec 16, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143562
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.