K-number	K173614
Device name	Penumbra Coil 400, Ruby Coil System, POD System
Applicant	Penumbra, Inc.
Product code	HCG
Device class	Class II
Decision date	Apr 17, 2018
Decision	Substantially Equivalent
Regulation	882.5950

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Source

View the full FDA submission: accessdata.fda.gov

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Penumbra Coil 400, Ruby Coil System, POD System

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