FDA 510(k) Applications Submitted by MICROVENA CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K991194	04/08/1999	MODIFICATION TO ULTRA-SELECT GUIDEWIRE	MICROVENA CORP.
K991898	06/04/1999	ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE	MICROVENA CORP.
K971984	05/29/1997	AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200)	MICROVENA CORP.
K972511	07/03/1997	AMPLATZ GOOSE NECK SNARE KIT/ CATHETER	MICROVENA CORP.
K954205	09/07/1995	THE AMPLATZ THROMBECTOMY DEVICE	MICROVENA CORP.
K954642	10/10/1995	HYDRO-SELECT GUIDEWIRE	MICROVENA CORP.
K955304	11/20/1995	CRICKET	MICROVENA CORP.
K970668	02/24/1997	THE AMPLANTZ GOOSE NECK MICROSNARE	MICROVENA CORP.
K982657	07/30/1998	AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100	MICROVENA CORP.