510(k) K001744 ยท MND Ligator, Esophageal
OLYMPUS ENDOSCOPIC LIGATION DEVICE
| Applicant | Olympus America, Inc., Melville NY, US |
| Decision | Substantially Equivalent, Feb 27, 2001 |
| Received | Jun 8, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001744
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.