Last synced on 25 January 2026 at 3:41 am

OMNI-DL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080650
510(k) Type
Traditional
Applicant
Transvivo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
264 days
Submission Type
Summary

OMNI-DL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080650
510(k) Type
Traditional
Applicant
Transvivo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
264 days
Submission Type
Summary