510(k) K971148 ยท MKJ Automated External Defibrillators (Non-Wearable)
700-SP SERIES DISPOSABLE STIMULATION ELECTRODES
| Applicant | Cardiotronics Systems, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 15, 1997 |
| Received | Mar 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971148
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.