510(k) K905276 ยท LKX Device, Thermal, Hemorrhoids
THERMA-H
| Applicant | Kure Swiss Medical AG Corp., Miami FL, US |
| Decision | Substantially Equivalent, Nov 7, 1991 |
| Received | Nov 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905276
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.