510(k) K033642 ยท MKJ Automated External Defibrillators (Non-Wearable)
SMARTLANK WIRELESS, MODEL 001970
| Applicant | Mrl, A Welch Allyn Company, Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, May 25, 2004 |
| Received | Nov 20, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033642
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.