Medical Device Manufacturer · US , San Diego , CA

Persyst Development Corporation - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2014

Total

Cleared

Denied

Persyst Development Corporation has 6 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Jan 2025. Active since 2014. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Persyst Development Corporation Filter by specialty or product code using the sidebar.

Persyst Development Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Persyst Development Corporation

6 devices

1-6 of 6