510(k) K140740 ยท DPW Flowmeter, Blood, Cardiovascular
TRANSONIC TISSUE PERFUSION MONITOR
| Applicant | Transonic Systems, Inc., Ithaca NY, US |
| Decision | Substantially Equivalent, Jul 23, 2015 |
| Received | Mar 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140740
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.