Solaris Medical Technology, Inc. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solaris Medical Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103, SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFS, SOLARIS MODELS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
5
Total
5
Cleared
0
Denied
Solaris Medical Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 5 cleared submissions from 2007 to 2010. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Solaris Medical Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Solaris Medical Technology, Inc.
5 devices
Cleared
Oct 07, 2010
NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103
Anesthesiology
268d
Cleared
Jul 22, 2010
SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFS
Cardiovascular
9d
Cleared
Mar 12, 2010
SOLARIS MODELS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
Anesthesiology
169d
Cleared
Jul 25, 2008
SOLARIS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
Anesthesiology
249d
Cleared
Jan 31, 2007
SOLARIS COMPATIBLE REUSABLE ADULT SPO2 FINGER SENSORS, MODELS S100A-090103...
Anesthesiology
208d