Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K982336 |
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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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Kuschall K Junior Manual wheelchair | 2 | 11/25/2009 | Invacare Corporation |
Kuschall''s K3/K4 Series of Manual Wheelchair, Model Airlite. | 2 | 09/06/2006 | Invacare Corporation |
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