510(k) K900581 ยท JFA Exerciser, Finger, Powered
DANNIFLEX CPM 880(TM)
| Applicant | Buckman Co., Inc., Concord CA, US |
| Decision | Substantially Equivalent, Feb 20, 1990 |
| Received | Feb 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900581
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.