Last synced on 9 May 2025 at 11:05 pm

ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100704
510(k) Type
Special
Applicant
DISETRONIC MEDICAL SYSTEMS AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
63 days
Submission Type
Summary

ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100704
510(k) Type
Special
Applicant
DISETRONIC MEDICAL SYSTEMS AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
63 days
Submission Type
Summary