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General Devices

13 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
EMS TELEMEDICINE OPTION (FOR GEMS SERIES 4000) (K013533)General Devices2002-01-18
ROSETTA-LT/ROSETTA-RX (K002089)General Devices2000-11-21
EIM-107 PREP-CHECK (K993202)General Devices1999-12-17
GEMSCOM SERIES 6000, MODELS 6100, 6200 & 6300 (K940009)General Devices1995-04-14
GEMSCOM SERIES 5000, (K935839)General Devices1994-11-10
GEMSCOM SERIES 300 12-LEAD ECG (12-LEAD OPTION) (K921929)General Devices1992-09-18
GEMSCOM SERIES 3000 (K914889)General Devices1992-03-04
TRU-VIEW MULTI-CHANNEL DISPLAY (K912008)General Devices1991-10-09
MODIFIED DR-2C/PMC 100 (K896153)General Devices1990-01-19
DR-2C (MODIFICATION) (K862596)General Devices1986-09-26
DR-2C (K844650)General Devices1985-01-22
AP-CHECK (K830877)General Devices1983-06-08
PREP-CHECK (K830876)General Devices1983-05-18

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Every clearance here is in the API, with alerts when new ones post.