510(k) K812567 ยท LKX Device, Thermal, Hemorrhoids
RELIEF
| Applicant | American Pharmaceutical Co., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 10, 1981 |
| Received | Sep 9, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812567
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.