FDA 510(k) Applications Submitted by B & J Manufacturing Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K200154 01/22/2020 B&J DVT Compression Devices MHH800/MHH800SQ B & J Manufacturing Ltd.
K201532 06/08/2020 B&J DVT Calf/Thigh Garments, Models 801/830 Series B & J Manufacturing Ltd.


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