FDA 510(k) Applications Submitted by ENVITEC-WISMAR GMBH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070193	01/22/2007	ENVITEC OXIPEN PULSE OXIMETER AND ACCESSORIES	ENVITEC-WISMAR GMBH
K090438	02/20/2009	REUSABLE ENVITEC FINGER SPO2 SENSOR-HP/PHILIPS COMPATIBLE, MODELS F-2412, F-2414-15, REUSABLE ENVITEC EAR SPO2 SENSOR	ENVITEC-WISMAR GMBH
K060675	03/14/2006	ENVITEC REUSABLE SOFTIP Y SPO2 SENSORS	ENVITEC-WISMAR GMBH
K122290	07/30/2012	ENVITEC MYSIGN O OXYGEN MEASURING DEVICE	ENVITEC-WISMAR GMBH
K102270	08/10/2010	ENVITEC REUSABLE SPO2 SENSORS TYPE NIHON-KOHDEN	ENVITEC-WISMAR GMBH
K082655	09/12/2008	ENVITEC MEDICAL OXYGEN SENORS, MODELS OOM101; 00M102/-1;OOM103/-1/-1M;OOM104;OOM105;00M106	ENVITEC-WISMAR GMBH
K133064	09/27/2013	MYSIGN S PULSE OXIMETER, MYSIGN PC SOFTWARE (OPTIONAL), SOFTTIP LARGE R-3211-31, FINGER CLIP F-3211-31	ENVITEC-WISMAR GMBH
K043463	12/15/2004	ENVITEC REUSABLE MULTI-SITE Y SPO2 SENSORS	ENVITEC-WISMAR GMBH
K992215	07/01/1999	MULTICOMPATIBLE ENVITEC FINGER CLIP SENSOR, MULTICOMPATIBLE ENVITEC ADULT DISPOSABLE SENSOR, MULTICOMPATIBLE ENVITEC PED	ENVITEC-WISMAR GMBH