Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K052057 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/... | 2 | 04/01/2020 |
FEI # 3015876 Physio-Control, Inc. |
| The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a paten... | 2 | 07/19/2013 |
FEI # 3015876 Physio Control, Inc. |
| The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a paten... | 2 | 07/26/2011 |
FEI # 3015876 Physio Control, Inc. |
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