510(k) K844388 ยท IPF Stimulator, Muscle, Powered
ESCOTEK EST 220 INTERFERENCE THERAPY UNIT
| Applicant | Nor-Am Patient Care Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 7, 1985 |
| Received | Nov 13, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844388
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.