Last synced on 25 January 2026 at 3:41 am

INTER-VIAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010703
510(k) Type
Traditional
Applicant
Duoject Medical Systems, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/25/2001
Days to Decision
108 days
Submission Type
Summary

INTER-VIAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010703
510(k) Type
Traditional
Applicant
Duoject Medical Systems, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/25/2001
Days to Decision
108 days
Submission Type
Summary