FDA 510(k) Applications for Medical Device Product Code: DTG (Magnet, Test, Pacemaker)

FDA 510(k) Applications for Medical Device Product Code "DTG"
(Magnet, Test, Pacemaker)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960849	CARDIAC ASSIST DEVICES, INC.	MAGNO ALARM	03/26/1997
K092364	CYBERONICS, INC.	MODEL 220 PATIENT MAGNET	11/03/2009

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