• 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 calculator, drug dose
510(k) Number K170669
Device Name Insulia Diabetes Management Companion
Voluntis S.A.
58, Avenue de Wagram
Paris,  FR 75017
Applicant Contact Raffi Krikorian
Voluntis S.A.
58, Avenue de Wagram
Paris,  FR 75017
Correspondent Contact Raffi Krikorian
Regulation Number868.1890
Classification Product Code
Date Received03/06/2017
Decision Date 06/19/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls