510(k) K023713 ยท KRC Tester, Electrode, Surface, Electrocardiographic
SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000
| Applicant | Sontra Medical, Inc., Cambridge MA, US |
| Decision | Substantially Equivalent, Jan 28, 2004 |
| Received | Nov 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023713
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.