510(k) K955890 ยท MKJ Automated External Defibrillators (Non-Wearable)
FIRST MEDIC PULSE OXIMETRY MODULE
| Applicant | Colorado Medtech, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Jul 28, 1997 |
| Received | Dec 29, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955890
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.