K-number	K222242
Device name	FloPatch FP120
Applicant	Flosonics Medical
Product code	DPW
Device class	Class II
Decision date	Dec 9, 2022
Decision	Substantially Equivalent
Regulation	870.2100

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Source

View the full FDA submission: accessdata.fda.gov

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FloPatch FP120

Everything you need for a 510(k) submission. Nothing you don't.