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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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