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
K895110 CARDIAC CONTROL SYSTEMS, INC. MAESTRO PACEMAKER TEST MAGNET 09/26/1989
K092364 CYBERONICS, INC. MODEL 220 PATIENT MAGNET 11/03/2009
K831926 OSCOR INC. IMPLANTABLE ENDOCARDIAL PACING LEADS 03/12/1984
K813153 PACESETTER SYSTEMS TEST MAGNET 12/02/1981


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