Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K012428 |
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Results per Page |
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 | Physio-Control, Inc. |
LIFEPAK 500 automated external defibrillator | 2 | 07/20/2004 | Medtronic Physio Control Corp |
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