510(k) K901849 ยท IPF Stimulator, Muscle, Powered
LUMISCOPE EMS 8000
| Applicant | Lumiscope Co., Inc., Edison NJ, US |
| Decision | Substantially Equivalent, Aug 24, 1990 |
| Received | Apr 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901849
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.