510(k) K010207 ยท MKJ Automated External Defibrillators (Non-Wearable)
PORTABLE INSTENSIVE CARE UNIT
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 14, 2001 |
| Received | Jan 23, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010207
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.