Medical Device Recalls
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1 result found
510(K) Number: K040012 |
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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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The Well@Home Monitor by Patient Care technologies Model 179-2150 Intended to be used as a clini... | 2 | 08/03/2010 | Zoe Medical Incorporated |
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