510(k) K981428 ยท LKX Device, Thermal, Hemorrhoids
ANU ICE
| Applicant | Cryoptherapy Pain Relief Products, Inc., Pembroke Pines FL, US |
| Decision | Substantially Equivalent, Jul 7, 1998 |
| Received | Apr 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981428
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.