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
FDA 510(k) Regulatory Record - Solaris Medical Technology, Inc. Anesthesiology ✕
4 devices
Cleared
Oct 07, 2010
NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103
Anesthesiology
268d
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