Last synced on 25 January 2026 at 3:41 am

ULTRAVIEW DM3 MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093802
510(k) Type
Traditional
Applicant
Zoe Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2010
Days to Decision
119 days
Submission Type
Summary

ULTRAVIEW DM3 MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093802
510(k) Type
Traditional
Applicant
Zoe Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2010
Days to Decision
119 days
Submission Type
Summary