510(k) K945221 ยท BXB Exerciser, Powered
SUTTER MODEL 6000 HAND CPM DEVICE
| Applicant | Sutter Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 27, 1995 |
| Received | Oct 26, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945221
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.