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

FDA 510(k) Number Submission Date Device Name Applicant
K250348 02/06/2025 JLK-AILink JLK, Inc.
K242556 08/28/2024 JLK-CTP JLK, Inc.
K242709 09/09/2024 JLK-PWI JLK, Inc.
K243363 10/29/2024 JLK-ICH JLK, Inc.
K243611 11/22/2024 JLK-SDH JLK, Inc.
K241480 05/24/2024 JBS-LVO JLK, Inc.


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