FDA 510(k) Applications for Medical Device Product Code "DOX"
(Fluorometer, Lead (Dedicated Instruments))

FDA 510(k) Number Applicant Device Name Decision Date
K832030 ARGON MEDICAL CORP. HEPARIN COATED STAINLESS STEEL/TEFLON 09/29/1983
K014195 BOSTON SCIENTIFIC CORP. KAYAK HYDROPHILIC GUIDE WIRES 03/19/2002
K944226 MSI, INC. MSI PROCEDURE KIT 06/21/1995
K900822 NATIONAL-STANDARD MEDICAL PRODUCTS HYDRO-SIL(TM) COATED GUIDEWIRES 07/17/1990


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