FDA 510(k) Applications Submitted by WESCOR, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K121823 06/21/2012 CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRIC WESCOR, INC.
K010031 01/03/2001 NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM WESCOR, INC.


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