General Devices
General Devices holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2002.
Top product codes for General Devices
Recent clearances by General Devices
- K013533 — EMS TELEMEDICINE OPTION (FOR GEMS SERIES 4000)
- K002089 — ROSETTA-LT/ROSETTA-RX
- K993202 — EIM-107 PREP-CHECK
- K940009 — GEMSCOM SERIES 6000, MODELS 6100, 6200 & 6300
- K935839 — GEMSCOM SERIES 5000,
- K921929 — GEMSCOM SERIES 300 12-LEAD ECG (12-LEAD OPTION)
- K914889 — GEMSCOM SERIES 3000
- K912008 — TRU-VIEW MULTI-CHANNEL DISPLAY
- K896153 — MODIFIED DR-2C/PMC 100
- K862596 — DR-2C (MODIFICATION)
- K844650 — DR-2C
- K830877 — AP-CHECK
- K830876 — PREP-CHECK
Data sourced from openFDA. This site is unofficial and independent of the FDA.