ClearanceBrief
Company ยท US

Persyst Development Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2025. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OMBAutomatic Event Detection Software For Full-Montage Electroencephalograph9
GWSAnalyzer, Spectrum, Electroencephalogram Signal1
GXZElectrode, Needle1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 31, 2025K252160Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))
Persyst Development, LLC
OMB
Jan 22, 2025K242446Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))
Persyst Development Corporation
OMB
Dec 30, 2022K222002Persyst 15 EEG Review and Analysis Software
Persyst Development Corporation
OMB
Nov 29, 2018K182181Persyst 14 EEG Review and Analysis Software
Persyst Development Corporation
OMB
Sep 21, 2017K171184Persyst Mobile App
Persyst Development Corporation
OMB
Aug 12, 2015K151929PERSYST 13 (P13) EEG REVIEW AND ANALYSIS SOFTWARE
Persyst Development Corporation
OMB
May 19, 2014K133793PERSYST 12 ( P12) EGG REVIEW AND ANALYSIS SOFTWARE
Persyst Development Corporation
OMB
Nov 21, 2013K132306PERSYST 12 EEG REVIEW AND ANALYSIS SOFTWARE
Persyst Development Corp.
OMB
Dec 8, 2011K103103PRESSON ELECTRODE
Persyst Development Corp.
GXZ
Aug 3, 2001K011397PERSYST REVEAL
Persyst Development Corp.
OMB
Mar 9, 1998K974718PERSYST PRISM
Persyst Development Corp.
GWS

Latest recalls

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