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FDA 510(k) Applications Submitted by PERSYST DEVELOPMENT CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K132306
07/24/2013
PERSYST 12 EEG REVIEW AND ANALYSIS SOFTWARE
PERSYST DEVELOPMENT CORP.
K011397
05/07/2001
PERSYST REVEAL
PERSYST DEVELOPMENT CORP.
K103103
10/20/2010
PRESSON ELECTRODE
PERSYST DEVELOPMENT CORP.
K974718
12/17/1997
PERSYST PRISM
PERSYST DEVELOPMENT CORP.
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