Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132251 |
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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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Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 Product Usage: The Panther instrument is... | 2 | 02/12/2018 | Hologic, Inc |
Panther(R) System, Catalog Number 902615, For Use with Hologic Assays, For In Vitro Diagnostic Use | 2 | 10/18/2017 | Hologic, Inc |
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