510(k) K152134 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Reprocessed Vessel Sealer
| Applicant | Sterilmed, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 15, 2016 |
| Received | Jul 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152134
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.