510(k) K984582 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX
| Applicant | Bio-Detek, Inc., Pawtucket RI, US |
| Decision | Substantially Equivalent, Mar 16, 1999 |
| Received | Dec 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984582
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.