Medical Device Recalls
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1 result found
510(K) Number: K123290 |
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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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Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e... | 2 | 09/15/2018 | Permobil, Ab |
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