Medical Device Recalls
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1 result found
510(K) Number: K984447 |
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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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Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to... | 2 | 02/04/2013 | Invacare Corporation |
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