Medical Device Recalls
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1 result found
510(K) Number: K090268 |
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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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0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system in order to take general... | 2 | 11/08/2012 | Shimadzu Medical Systems |
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