510(k) K061606 ยท DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
DEFIBRILLATOR CABLE TESTER, MODEL DT2200
| Applicant | Medical Devices/Padpro, Inc., Deer Field IL, US |
| Decision | Substantially Equivalent, Jun 21, 2006 |
| Received | Jun 9, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061606
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.