510(k) K013803 ยท DPW Flowmeter, Blood, Cardiovascular
FLOWGUARD DEVICE
| Applicant | Biosonix , Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Feb 13, 2002 |
| Received | Nov 15, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013803
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.