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.

FDA 510(k) Regulatory Record - Persyst Development Corporation

6 devices

1-6 of 6