FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

CareSens S Fit Blood Glucose Monitoring System

K Number: K180866 · Decision Aug 31, 2018
Classifications
1
FEI Numbers
168
Registration Numbers
169
Same Product Code
507
Applicant Total
27
Review Days
151

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Basic Information

Device Name
CareSens S Fit Blood Glucose Monitoring System
K Number
K180866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
I-Sens, Inc.
Date Received
April 2, 2018
Decision Date
August 31, 2018
Product Code
NBW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NBW System, Test, Blood Glucose, Over The Counter

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Other Clearances by I-Sens, Inc.

K Number Device Name
K230625 ReliOn Premier BLU Blood Glucose Monitoring System
K222656 LDE4 Lancing Device
K201394 CareSens N Feliz Blood Glucose Monitoring System, CareSens N Feliz BT Blood Glucose Monitoring System
K201551 KetoSens BT Blood B-Ketone Monitoring System
K192859 CareSens S Clear BT Blood Glucose Monitoring System
K193590 CareSens S Fit BT Blood Glucose Monitoring System
K192220 ReliOn Premier Classic Blood Glucose Monitoring System
K181273 GLUCOCARD Shine Connex Blood Glucose Monitoring System, GLUCOCARD Shine Express Blood Glucose Monitoring System
K170463 KetoSens Blood B-Ketone Monitoring System, KetoSens Multi Blood B-Ketone Monitoring System
K171480 NoCoding1 Plus Blood Glucose Monitoring System, VeraSens Blood Glucose Monitoring System
Search all 27 clearances from I-Sens, Inc. →