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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