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FDA 510(k) Applications Submitted by StimLabs, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231325
05/08/2023
Corplex P / Theracor P / Allacor P
StimLabs, LLC
K242828
09/19/2024
Corplex P/ Theracor P/ Allacor P
StimLabs, LLC
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