510(k) K081450

RIGHTEST BLOOD GLUCOSE MONITORING SYSTEM, MODEL GM110 by Bionime Corporation — Product Code NBW

K081450 is an FDA 510(k) premarket notification submitted by Bionime Corporation for the device "RIGHTEST BLOOD GLUCOSE MONITORING SYSTEM, MODEL GM110". The FDA issued a decision of Substantially Equivalent on September 11, 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. Bionime Corporation has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 2008
Date Received
May 23, 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