510(k) K012030 ยท MKJ Automated External Defibrillators (Non-Wearable)
PORTABLE INTENSIVE CARE UNIT
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Sep 24, 2001 |
| Received | Jun 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012030
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.