Persyst Development, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Persyst Development, LLC - FDA 510(k) Cleared Devices
Recent clearances: Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))
1
Total
1
Cleared
0
Denied
Persyst Development, LLC has 1 FDA 510(k) cleared medical devices. Based in Solana Beach, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Persyst Development, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Persyst Development, LLC
1 devices