510(k) K033424 ยท DPW Flowmeter, Blood, Cardiovascular
ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002
| Applicant | Transonic Systems, Inc., Ithaca NY, US |
| Decision | Substantially Equivalent, Dec 11, 2003 |
| Received | Oct 23, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033424
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.