Last synced on 25 January 2026 at 3:41 am

DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013782
510(k) Type
Traditional
Applicant
Disetronic Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
6 days
Submission Type
Summary

DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013782
510(k) Type
Traditional
Applicant
Disetronic Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
6 days
Submission Type
Summary