510(k) K023431 ยท DPW Flowmeter, Blood, Cardiovascular
QUANTIX/ND DEVICE
| Applicant | Cardiosonix, Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Nov 13, 2002 |
| Received | Oct 15, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023431
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.