K-number	K933517
Device name	AUTOMATIC PULL BACK DEVICE
Applicant	Cardiovascular Imaging Systems, Inc.
Product code	DQX
Device class	Class II
Decision date	Oct 15, 1993
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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AUTOMATIC PULL BACK DEVICE

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