510(k) K984255 ยท MND Ligator, Esophageal
OLYMPUS HX-20 SERIES LIGATING DEVICE
| Applicant | Olympus Corp of America, Lake Success NY, US |
| Decision | Substantially Equivalent, Jan 12, 1999 |
| Received | Nov 30, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984255
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.