Medical Device Recalls
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1 result found
510(K) Number: K962781 |
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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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Model 511 Cardio Respiratory Monitor with Oximax technology with software version 5.0 | 2 | 07/20/2004 | CAS Medical Systems, Inc. |
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