510(k) K854569 ยท LKX Device, Thermal, Hemorrhoids
HEMOR-ICE
| Applicant | Technology 2000, Lakewood NJ, US |
| Decision | Substantially Equivalent, Feb 5, 1986 |
| Received | Nov 14, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854569
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.