FDA 510(k) Applications Submitted by JENNIFER TRIBETT

FDA 510(k) Number Submission Date Device Name Applicant
K011145 03/26/2001 MODIFICATION TO REFLOTRON AMYLASE, CAT. 1200658 ROCHE DIAGNOSTICS CORP.
K013373 10/11/2001 OMNI C ANALYZER ROCHE DIAGNOSTICS CORP.


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