510(k) K983307 ยท MKJ Automated External Defibrillators (Non-Wearable)
MODIFICATION TO PORTABLE INTENSIVE CARE UNIT
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Nov 20, 1998 |
| Received | Sep 21, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983307
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.