Medical Device Recalls
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1 result found
510(K) Number: K103732 |
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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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| Ambulatory Blood Pressure (ABP) Monitor, Model 90217A. The Spacelabs Model 90217A Ambulatory Bloo... | 2 | 11/29/2011 |
FEI # 3002807992 Del Mar Reynolds Medical, Ltd. |
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