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Persyst Development Corporation

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories1
Latest FDA decision2025-01-22
TypeNumberDevice NameCodeDateActions
510(k) K242446 Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))OMB2025-01-22 View
510(k) K222002 Persyst 15 EEG Review and Analysis SoftwareOMB2022-12-30 View
510(k) K182181 Persyst 14 EEG Review and Analysis SoftwareOMB2018-11-29 View
510(k) K171184 Persyst Mobile AppOMB2017-09-21 View