Envitec-Wismar GmbH - FDA 510(k) Cleared Devices
Recent clearances: MYSIGN S PULSE OXIMETER, MYSIGN PC SOFTWARE (OPTIONAL), SOFTTIP LARGE R-3211-31, FINGER CLIP F-3211-31, ENVITEC MYSIGN O OXYGEN MEASURING DEVICE, ENVITEC REUSABLE SPO2 SENSORS TYPE NIHON-KOHDEN
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Envitec-Wismar GmbH Anesthesiology ✕
9 devices
Cleared
May 02, 2014
MYSIGN S PULSE OXIMETER, MYSIGN PC SOFTWARE (OPTIONAL), SOFTTIP LARGE...
Anesthesiology
217d
Cleared
Jan 23, 2013
ENVITEC MYSIGN O OXYGEN MEASURING DEVICE
Anesthesiology
177d
Cleared
Feb 22, 2011
ENVITEC REUSABLE SPO2 SENSORS TYPE NIHON-KOHDEN
Anesthesiology
196d
Cleared
Jul 24, 2009
REUSABLE ENVITEC FINGER SPO2 SENSOR-HP/PHILIPS COMPATIBLE, MODELS F-2412,...
Anesthesiology
154d
Cleared
Nov 25, 2008
ENVITEC MEDICAL OXYGEN SENORS, MODELS OOM101
Anesthesiology
74d
Cleared
May 02, 2007
ENVITEC OXIPEN PULSE OXIMETER AND ACCESSORIES
Anesthesiology
100d
Cleared
Jul 17, 2006
ENVITEC REUSABLE SOFTIP Y SPO2 SENSORS
Anesthesiology
125d
Cleared
Feb 11, 2005
ENVITEC REUSABLE MULTI-SITE Y SPO2 SENSORS
Anesthesiology
58d
Cleared
Mar 29, 2000
MULTICOMPATIBLE ENVITEC FINGER CLIP SENSOR, MULTICOMPATIBLE ENVITEC ADULT...
Anesthesiology
272d