K-number	K233391
Device name	cCeLL - In vivo
Applicant	VPIX Medical, Inc.
Product code	GWG
Device class	Class II
Decision date	Aug 21, 2024
Decision	Substantially Equivalent
Regulation	882.1480

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Source

View the full FDA submission: accessdata.fda.gov

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cCeLL - In vivo

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