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ULTRA DCI MODEL 5000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100363
510(k) Type
Traditional
Applicant
Ultrasound Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2010
Days to Decision
98 days
Submission Type
Summary

ULTRA DCI MODEL 5000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100363
510(k) Type
Traditional
Applicant
Ultrasound Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2010
Days to Decision
98 days
Submission Type
Summary