K-number	K202821
Device name	Indigo Aspiration System - Aspiration Catheter 12 and Separator 12
Applicant	Penumbra, Inc.
Product code	QEW
Device class	Class II
Decision date	Nov 18, 2020
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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Indigo Aspiration System - Aspiration Catheter 12 and Separator 12

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