510(k) K921207 ยท DRX Electrode, Electrocardiograph
DRIGEL DEFIBRILLATOR/SYNCHRONIZED COARDIOVERSION
| Applicant | Physiometrix, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Oct 13, 1992 |
| Received | Mar 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921207
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.