K-number	K231325
Device name	Corplex P / Theracor P / Allacor P
Applicant	Stimlabs, LLC
Product code	KGN
Device class	Class U
Decision date	Feb 2, 2024
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Corplex P / Theracor P / Allacor P

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