510(k) K010253 ยท DYG Catheter, Flow Directed
ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101
| Applicant | Transonic Systems, Inc., Ithaca NY, US |
| Decision | Substantially Equivalent, Mar 19, 2002 |
| Received | Jan 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010253
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.