FDA 510(k) Applications Submitted by MIMVISTA CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K060816 03/27/2006 MIM 4.0 (NEURO MIMVISTA CORP.
K071964 07/16/2007 MIM 4.1 (SEASTAR) MIMVISTA CORP.
K062163 07/28/2006 MIMVIEWER MIMVISTA CORP.
K052379 08/30/2005 MIM 3.5 (CIRCA) MIMVISTA CORP.


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