510(k) K082486

GLUCOFACTS EXPRESS DIABETES MANAGEMENT SOFTWARE by Bayer Healthcare, LLC — Product Code NBW

K082486 is an FDA 510(k) premarket notification submitted by Bayer Healthcare, LLC for the device "GLUCOFACTS EXPRESS DIABETES MANAGEMENT SOFTWARE". The FDA issued a decision of Substantially Equivalent on October 8, 2008. The device falls under product code NBW (System, Test, Blood Glucose, Over The Counter), a Class II device regulated under 21 CFR 862.1345. Bayer Healthcare, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 8, 2008
Date Received
August 28, 2008
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Blood Glucose, Over The Counter
Device Class
Class II
Regulation Number
862.1345
Review Panel
CH
Submission Type