K-number	K093969
Device name	ACUITY BREAK-AWAY GUIDE CATHETER
Applicant	Cardiac Pacemakers, Inc.
Product code	DQY
Device class	Class II
Decision date	Mar 5, 2010
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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ACUITY BREAK-AWAY GUIDE CATHETER

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