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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K991658
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Product Description
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FDA Recall
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Permobil Chairman 2K powered wheelchair 2 05/15/2003 Permobile Inc.
Permobil Chairman 2K powered wheelchair, Model 1280 2 03/21/2003 Permobile Inc.
Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e... 2 09/15/2018 Permobil, Ab
Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 2 10/03/2017 Permobil, Ab
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR... 2 10/03/2017 Permobil, Ab
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