K-number	K142870
Device name	Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]
Applicant	Penumbra, Inc.
Product code	QEW
Device class	Class II
Decision date	May 26, 2015
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]

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