K-number	K180939
Device name	Indigo Aspiration System - Modified 110 Aspiration Tubing
Applicant	Penumbra, Inc.
Product code	QEW
Device class	Class II
Decision date	May 3, 2018
Decision	Substantially Equivalent
Regulation	870.5150

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Source

View the full FDA submission: accessdata.fda.gov

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Indigo Aspiration System - Modified 110 Aspiration Tubing

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