510(k) K050088 ยท DPW Flowmeter, Blood, Cardiovascular
QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER
| Applicant | Neoprobe Corp., Dublin OH, US |
| Decision | Substantially Equivalent, Feb 8, 2005 |
| Received | Jan 13, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050088
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.