Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems
510(k) Number K213996
Device Name FreeStyle Libre 3 Continuous Glucose Monitoring System
Applicant
Abbott Diabetes Care Inc.
1360 South Loop Road
Alameda,  CA  94502
Applicant Contact Rodney Huang
Correspondent
Abbott Diabetes Care Inc.
1360 South Loop Road
Alameda,  CA  94502
Correspondent Contact Rodney Huang
Regulation Number862.1355
Classification Product Code
QLG  
Date Received12/20/2021
Decision Date 05/26/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-