Vega Technologies, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Vega Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 6 cleared submissions from 2001 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vega Technologies, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jun 10, 2011
VEGA CPAP SYSTEM/HEATED HUMIDIFIER, MODEL CP-03
Anesthesiology
270d
Cleared
Jan 14, 2011
INFRARED EAR THERMOMETER, MODEL IR-04MT
General Hospital
102d
Cleared
Nov 12, 2010
VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01
General & Plastic Surgery
60d
Cleared
Sep 08, 2004
DIGITAL THERMOMETER, MODELS MT-XX8 AND MT-XX9
General Hospital
96d
Cleared
Oct 07, 2003
VIGORMIST COMPRESSOR NEBULIZER
Anesthesiology
155d
Cleared
May 23, 2001
VEGA ULTRASONIC NEBULIZER
Anesthesiology
254d