Microvision Incorporated is one of 25845 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microvision Incorporated - FDA 510(k) Cleared Devices
Recent clearances: NOMAD ND1000M AUGMENTED VISION SYSTEM
1
Total
1
Cleared
0
Denied
Microvision Incorporated has 1 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Microvision Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microvision Incorporated
1 devices