K-number	K183120
Device name	EmboCube Embolization Gelatin
Applicant	Biosphere Medical, S.A.
Product code	KRD
Device class	Class II
Decision date	Aug 6, 2019
Decision	Substantially Equivalent
Regulation	870.3300

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Source

View the full FDA submission: accessdata.fda.gov

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EmboCube Embolization Gelatin

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