510(k) K041180 ยท DPW Flowmeter, Blood, Cardiovascular
QUANTIX OR VESSEL STABILIZER DEVICE
| Applicant | Cardiosonix, Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Jun 7, 2004 |
| Received | May 6, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041180
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.