Medical Device Recalls
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1 result found
510(K) Number: K083503 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DRAD-3000E: Radrex-i X-ray is a general purpose X-ray System. Labeling reads in part "TOSHIBA***DIG... | 2 | 02/02/2012 |
FEI # 2020563 Toshiba American Medical Systems Inc |
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