510(k) K820742 ยท DPW Flowmeter, Blood, Cardiovascular
NIHON KOHDEN BLOOD FLOWMETERS #MFV-1100
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Apr 15, 1982 |
| Received | Mar 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820742
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.