Medical Device Recalls
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1 result found
510(K) Number: K123828 |
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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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Prosound F75 or F75 The Hitachi Aloka Medical, Ltd. Prosound F75 is intended for use by trained per... | 2 | 03/29/2017 | Hitachi Aloka Medical, Ltd. |
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