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FDA 510(k) Applications Submitted by GENESIS INDUSTRIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K994361
12/27/1999
ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL
GENESIS INDUSTRIES, INC.
K962828
07/19/1996
EVERT-IT
GENESIS INDUSTRIES, INC.
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