510(k) K013939 ยท DPT Probe, Blood-Flow, Extravascular
JOSTRA FLOWPROBE FP-32E
| Applicant | Jostra AG, Oxford PA, US |
| Decision | Substantially Equivalent, Dec 14, 2001 |
| Received | Nov 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013939
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.