Medical Device Recalls
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1 result found
510(K) Number: K870176 |
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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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| Bio-Rad Pathfinder RSV Test Kit. Top of kit labeled PATHFINDER RSV DIRECT ANTIGEN DETECTION SYSTEM... | 2 | 03/29/2005 |
FEI # 3008272466 Bio Rad Laboratories, Inc. |
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