K-number	K913783
Device name	CORDIS PTCA GUIDING CATHETER, MODIFICATION
Applicant	Dow Corning Wright
Product code	DQY
Device class	Class II
Decision date	Oct 18, 1991
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CORDIS PTCA GUIDING CATHETER, MODIFICATION

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