K-number	K182522
Device name	Penumbra System (Modified 110 Aspiration Tubing)
Applicant	Penumbra, Inc.
Product code	NRY
Device class	Class II
Decision date	Oct 12, 2018
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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Penumbra System (Modified 110 Aspiration Tubing)

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