Medical Device Recalls
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1 result found
510(K) Number: K041202 |
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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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| McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30... | 3 | 03/30/2019 |
FEI # 1451040 Cypress Medical Products LLC |
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