510(k) K172093 ยท NLM Laparoscope, General & Plastic Surgery, Reprocessed
Reprocessed Covidien Trocar
| Applicant | Renovo, Inc., Bend OR, US |
| Decision | Substantially Equivalent, Oct 5, 2017 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172093
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.