Vega Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 6
- Compliance Actions
- 2
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K102625 | VEGA CPAP SYSTEM/HEATED HUMIDIFIER, MODEL CP-03 | June 10, 2011 |
| K102934 | INFRARED EAR THERMOMETER, MODEL IR-04MT | January 14, 2011 |
| K102626 | VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 | November 12, 2010 |
| K041516 | DIGITAL THERMOMETER, MODELS MT-XX8 AND MT-XX9 | September 8, 2004 |
| K031413 | VIGORMIST COMPRESSOR NEBULIZER | October 7, 2003 |
| K002831 | VEGA ULTRASONIC NEBULIZER | May 23, 2001 |