510(k) K070232 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)
ECG CABLES, TRUNK AND PATIENT LEAD WIRES
| Applicant | American I.V. Products, Inc., Harmans MD, US |
| Decision | Substantially Equivalent, Mar 27, 2007 |
| Received | Jan 24, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K070232
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.