Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K134046 |
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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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Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Densh... | 2 | 12/06/2017 | Fukuda Denshi Co., Ltd. |
Fukuda Denshi patient monitor model DS-8100M and DS-8100N. The Fukuda Denshi DynaScope Model DS-8... | 2 | 01/16/2016 | Fukuda Denshi USA, Inc. |
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