Vega Technologies, Inc. is one of 512 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Vega Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VEGA CPAP SYSTEM/HEATED HUMIDIFIER, MODEL CP-03, INFRARED EAR THERMOMETER, MODEL IR-04MT, VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01
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.
510(k) submissions have been managed by Center For Measurement Standards of Industrial as regulatory consultant.
FDA 510(k) Regulatory Record - Vega Technologies, Inc.
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