K-number	K843012
Device name	WIREGUIDE OR GUIDEWIRE
Applicant	Medi-Tech, Inc.
Product code	DQX
Device class	Class II
Decision date	Nov 29, 1984
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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WIREGUIDE OR GUIDEWIRE

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