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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K221438
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WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, ... 1 04/24/2026 FEI # 3021071770
WHILL, INC.
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