Medical Device Recalls
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1 result found
510(K) Number: K854079 |
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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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| Pacific Hemostasis brand SickleScreen Sickling Hemoglobin Screening Kit, Fisher Diagnostics catalog ... | 3 | 09/30/2004 |
FEI # 1181121 Fisher Diagnostic, A Company of Fisher Scientific LLC |
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