510(k) K822649 ยท LKX Device, Thermal, Hemorrhoids
DEVICE FOR THE TREATMENT OF HEMORRHOIDS
| Applicant | Dunmore Corp., Walker MI, US |
| Decision | Substantially Equivalent, Nov 3, 1982 |
| Received | Sep 1, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822649
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.