FDA 510(k) Application Details - K191450

Device Classification Name	More FDA Info for this Device
510(K) Number	K191450
Device Name	Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose Program Continuous Glucose Monitoring System and Dexcom Pro Q Continuous Glucose Monitoring System
Applicant	Dexcom, Inc. 6310 Sequence Dr. San Diego, CA 92121 US Other 510(k) Applications for this Company
Contact	Emily Chung Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QBJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2019
Decision Date	06/28/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review