FDA 510(k) Applications Submitted by Melissa O'Connor

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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