510(k) K840522 ยท DPW Flowmeter, Blood, Cardiovascular
RECOMED BLOOD-FLOW METER H236-052-02
| Applicant | Litton Medical Electronics, Elk Grove Village IL, US |
| Decision | Substantially Equivalent, May 16, 1985 |
| Received | Feb 7, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840522
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.