Medical Device Manufacturer · US , San Diego , CA

Medwaves Incorporated - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Medwaves Incorporated has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 3 cleared submissions from 2007 to 2015. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Medwaves Incorporated Filter by specialty or product code using the sidebar.

Medwaves Incorporated is one of 5008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medwaves Incorporated

3 devices

1-3 of 3