FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Dexcom G6 Pro Continuous Glucose Monitoring System

K Number: K191833 · Decision Oct 7, 2019
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
0
Applicant Total
27
Review Days
90

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Basic Information

Device Name
Dexcom G6 Pro Continuous Glucose Monitoring System
K Number
K191833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1355
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dexcom, Inc.
Date Received
July 9, 2019
Decision Date
October 7, 2019
Product Code
QII
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
QII Integrated Continuous Glucose Monitoring System For Professional Directed Retrospective Or Real-Time Use

Other Clearances by Dexcom, Inc.

K Number Device Name
K260935 Stelo Glucose Biosensor System
K261402 Dexcom G7 Continuous Glucose Monitoring System;Dexcom G7 15 Day Continuous Glucose Monitoring System
K261359 Stelo Glucose Biosensor System
K253737 Dexcom G7 Continuous Glucose Monitoring (CGM) System; Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System
K253710 Dexcom G7 Continuous Glucose Monitoring (CGM) System, Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System
K252818 Dexcom Smart Basal
K243214 Dexcom G7 15 Day Continuous Glucose Monitoring System
K240902 Dexcom G7 Continuous Glucose Monitoring System
K234070 Stelo Glucose Biosensor System
K234133 Dexcom G7 Continuous Glucose Monitoring System
Search all 27 clearances from Dexcom, Inc. →