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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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