Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K052500 |
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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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Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device... | 2 | 06/14/2018 | Shimadzu Medical Systems |
Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended to be u... | 2 | 05/08/2014 | Shimadzu Medical Systems |
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