FDA 510(k) Applications Submitted by Whill, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K153543 12/11/2015 WHILL Model M WHILL, INC.
K221438 05/17/2022 WHILL Model F Whill, Inc.
K213383 10/13/2021 WHILL Model C2 Whill, Inc.


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