K-number	K231539
Device name	pRESET LITE Thrombectomy Device
Applicant	Phenox Limited
Product code	POL
Device class	Class II
Decision date	Oct 21, 2023
Decision	Substantially Equivalent
Regulation	882.5600

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Source

View the full FDA submission: accessdata.fda.gov

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pRESET LITE Thrombectomy Device

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