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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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