Medical Device Recalls
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1 result found
510(K) Number: K093466 |
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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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Hitachi HIVISION Preirus/Avius Ultrasound equipped with V03.02 Software - Doppler Trace Measurement ... | 2 | 06/08/2011 | Hitachi Medical Systems America Inc |
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