Medical Device Recalls
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1 result found
510(K) Number: K120446 |
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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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Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images of submucosal and per... | 2 | 10/30/2013 | Fujinon Inc |
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