510(k) K173740 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Reprocessed DePuy Mitek Ablation Wand
| Applicant | Renovo, Inc., Bend OR, US |
| Decision | Substantially Equivalent, Mar 19, 2018 |
| Received | Dec 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173740
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.