K-number	K950855
Device name	ASE MAXI-TORQUE, SUPPLE FLEX ANGIOGRAPHIC CATHETERS
Applicant	Adam Spence Corp.
Product code	DQO
Device class	Class II
Decision date	May 30, 1995
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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ASE MAXI-TORQUE, SUPPLE FLEX ANGIOGRAPHIC CATHETERS

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