Medical Device Recalls
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1 result found
510(K) Number: K040637 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Powerheart AED G3 Automated External Defibrillator Model 9300P Professional series). Cardiac Scienc... | 2 | 01/15/2005 |
FEI # 2112020 Cardiac Science, Inc. |
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