FDA 510(k) Applications Submitted by BESTGEN BIOTECH CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K090389 02/17/2009 AP-1000 BLOOD GLUCOSE MONITORING SYSTEM BESTGEN BIOTECH CORP.
K072274 08/15/2007 MAJOR III BLOOD GLUCOSE MONITORING SYSTEM BESTGEN BIOTECH CORP.
K100437 02/17/2010 AP-1000 BLOOD GLUCOSE MONITORING SYSTEM, MODEL AP-1000, MAJOR GLUCOSE CONTROL SOLUTION BESTGEN BIOTECH CORP.
K103044 10/14/2010 AP-1010 AND AP-1020 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTION BESTGEN BIOTECH CORP.
K103116 10/21/2010 AP-2000, AP-2010, AND AP-2020 BLOOD GLUCOSE MONITORING SYSTEM BESTGEN BIOTECH CORP.
K103230 11/01/2010 AP-3000 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTION BESTGEN BIOTECH CORP.


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