510(k) K151567 ยท HFI Coagulator, Culdoscopic (And Accessories)
ENDOPLUS hand-held laparoscopic instruments
| Applicant | Endoplus, Mundelein IL, US |
| Decision | Substantially Equivalent, Dec 23, 2015 |
| Received | Jun 10, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151567
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.