K-number	K192413
Device name	SiteSeal Femoral Compression Device
Applicant	Ensite Vacular, LLC
Product code	DXC
Device class	Class II
Decision date	Mar 31, 2020
Decision	Substantially Equivalent
Regulation	870.4450

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Source

View the full FDA submission: accessdata.fda.gov

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SiteSeal Femoral Compression Device

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