510(k) K944874 ยท LKX Device, Thermal, Hemorrhoids
ZEROID HEMORRHOIDAL DEVICE
| Applicant | Medical Appliance Research Corp., North Miami Beach FL, US |
| Decision | Substantially Equivalent, Aug 7, 1995 |
| Received | Oct 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944874
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.