FDA 510(k), K093745, ONE TOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k), K093745, ONE TOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
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510(K) Number: K093745
Device Name: ONE TOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
Manufacturer:
Device Classification Name: System, Test, Blood Glucose, Over The Counter
Regulation Number: 862.1345
Classification Product Code: NBW
Date Received: 12/04/2009
Decision Date: 02/11/2011
Regulation Medical Specialty: Clinical Chemistry
Device Name: ONE TOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
Manufacturer:
Device Classification Name: System, Test, Blood Glucose, Over The Counter
Regulation Number: 862.1345
Classification Product Code: NBW
Date Received: 12/04/2009
Decision Date: 02/11/2011
Regulation Medical Specialty: Clinical Chemistry