510(k) K160742

NoCoding1 Plus Blood Glucose Monitoring System by I-Sens, Inc. — Product Code NBW

K160742 is an FDA 510(k) premarket notification submitted by I-Sens, Inc. for the device "NoCoding1 Plus Blood Glucose Monitoring System". The FDA issued a decision of Substantially Equivalent on December 16, 2016. The device falls under product code NBW (System, Test, Blood Glucose, Over The Counter), a Class II device regulated under 21 CFR 862.1345. I-Sens, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 16, 2016
Date Received
March 17, 2016
Clearance Type
Traditional
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