510(k) K141795 ยท MKJ Automated External Defibrillators (Non-Wearable)
BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500
| Applicant | R & D Batteries, Inc., Castle Rock CO, US |
| Decision | Substantially Equivalent, Dec 8, 2014 |
| Received | Jul 3, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141795
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.