Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173408 |
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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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MAMMOMAT Revelation, model no. 11343300 - Product Usage: is intended to be used for mammography exam... | 2 | 06/16/2020 | Siemens Medical Solutions USA, Inc |
Mammomat Revelation with software version VC10 and Biopsy Option Intended Use: For mammography ex... | 2 | 10/18/2019 | Siemens Medical Solutions USA, Inc |
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