510(k) K020743 ยท MKJ Automated External Defibrillators (Non-Wearable)
PADPRO, MODEL 2502
| Applicant | Padpro, LLC, Deer Field IL, US |
| Decision | Substantially Equivalent, May 28, 2002 |
| Received | Mar 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020743
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.