510(k) K955887 ยท DXW System, Phonocatheter, Intracavitary
NEWMED ABP-LITE
| Applicant | Newmed Corp., Washington DC, US |
| Decision | Substantially Equivalent, Sep 5, 1996 |
| Received | Dec 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955887
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.