Medical Device Recalls
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1 result found
510(K) Number: K925542 |
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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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Critikon brand Omni-Stat Finger Sensor - P/N 009084 | 2 | 10/15/2003 | GE Medical Systems Information Technologies |
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