510(k) K964991 ยท MKJ Automated External Defibrillators (Non-Wearable)
700-FR SERIES RADIOLUCENT STIMULATION ELECTRODES
| Applicant | Cardiotronics Systems, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 15, 1997 |
| Received | Dec 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964991
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.