Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K011987 |
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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 M-IV Mammography System; Model M4--00001. Intended to produce radiographic images of the ... | 2 | 06/03/2014 | Hologic, Inc. |
Lorad M-IV Mammography System | 2 | 08/11/2004 | Lorad, A Division of Hologic |
Lorad MIV Platinum Mammograpgy System | 2 | 08/11/2004 | Lorad, A Division of Hologic |
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