Medical Device Recalls
-
1 result found
510(K) Number: K122600 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/me... | 1 | 03/03/2017 | Physio-Control, Inc. |
-