Medical Device Recalls
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1 result found
510(K) Number: K895379 |
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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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| Physio-Control Internal Defibrillator Handles. PN: 3010901-002 for use with LIFEPAK 12 and 20. PN:... | 2 | 09/16/2008 |
FEI # 3015876 Physio Control, Inc. |
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