Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K944543 |
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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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| AxioBionics Wearable Therapy Upper Extremity BioSleeve (Right and Left) that includes 2-16 BioGel Ve... | 2 | 08/01/2011 |
FEI # 3008525454 Axiobionics, LLC |
| AxioBionics Wearable Therapy BioVest/Unitard that includes 2-16 BioGel Velcro Electrodes in sizes: 2... | 2 | 08/01/2011 |
FEI # 3008525454 Axiobionics, LLC |
| AxioBionics Wearable Therapy BioShorts that includes 2-16 BioGel Velcro Electrodes in sizes: 2"x2", ... | 2 | 08/01/2011 |
FEI # 3008525454 Axiobionics, LLC |
| AxioBionics Wearable TherapyFreeStep Sleeve (Right and Left) that includes 2-16 BioGel Velcro Electr... | 2 | 08/01/2011 |
FEI # 3008525454 Axiobionics, LLC |
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