K-number	K221070
Device name	DP4 Microneedling device
Applicant	Equipmed USA, LLC
Product code	QAI
Device class	Class II
Decision date	Dec 20, 2022
Decision	Substantially Equivalent
Regulation	878.4430

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Source

View the full FDA submission: accessdata.fda.gov

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DP4 Microneedling device

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