Medical Device Recalls
-
|
1 result found
510(K) Number: K111693 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The Hear... | 2 | 03/19/2014 |
FEI # 1000524572 Philips Medical Systems North America Inc. |
-







