Hoffrichter GmbH is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hoffrichter GmbH - FDA 510(k) Cleared Devices
Recent clearances: TREND 200 CPAP DEVICE, MODEL 5CP201, HOFFRICHTER TREND 110 CPAP DEVICE WITH AQUATREND III CPAP HUMIDIFIER ACCESSORY FOR TREND, HOFFRICHTER VECTOR, VECTOR PLUS, VECTOR BI-VEVEL, VECTOR BI-LEVEL PLUS, SCALAR, SCALAR PLUS
3
Total
3
Cleared
0
Denied
Hoffrichter GmbH has 3 FDA 510(k) cleared medical devices. Based in Egale, US.
Historical record: 3 cleared submissions from 2003 to 2006. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Hoffrichter GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hoffrichter GmbH
3 devices
Cleared
Jan 04, 2006
TREND 200 CPAP DEVICE, MODEL 5CP201
Anesthesiology
20d
Cleared
Jun 09, 2004
HOFFRICHTER TREND 110 CPAP DEVICE WITH AQUATREND III CPAP HUMIDIFIER...
Anesthesiology
49d
Cleared
Jul 23, 2003
HOFFRICHTER VECTOR, VECTOR PLUS, VECTOR BI-VEVEL, VECTOR BI-LEVEL PLUS,...
Anesthesiology
590d