Medical Device Recalls
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1 result found
510(K) Number: K111636 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Chenica Gunnell Rehab Series of Wheelchairs (GRSW); Mechanical Wheelchair, Sold as Rehab Tough and ... | 2 | 02/13/2013 |
FEI # 3009255757 CHENICA INC. |
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