510(k) K193590

CareSens S Fit BT Blood Glucose Monitoring System by I-Sens, Inc. — Product Code NBW

K193590 is an FDA 510(k) premarket notification submitted by I-Sens, Inc. for the device "CareSens S Fit BT Blood Glucose Monitoring System". The FDA issued a decision of Substantially Equivalent on January 17, 2020. 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
January 17, 2020
Date Received
December 23, 2019
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