FDA 510(k) Applications Submitted by VANCOUVER BIOTECH LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K050644 03/14/2005 VANCOUVER BIOTECH HUMAN CARDIAC TROPONIN I IMMUNOASSAY TEST KIT VANCOUVER BIOTECH LTD.
K023505 10/18/2002 VBL SERUM TROPONIN I TEST, MODEL 1001 VANCOUVER BIOTECH LTD.


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