510(k) K903633 ยท DPW Flowmeter, Blood, Cardiovascular
ADVANCE LASER FLOWMETER, ALF 21
| Applicant | Transonic Systems, Inc., Ithaca NY, US |
| Decision | Substantially Equivalent, Oct 9, 1990 |
| Received | Aug 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903633
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.