Last synced on 25 January 2026 at 3:41 am

CARDIOSCOPE SONOPLUS 3000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051126
510(k) Type
Traditional
Applicant
Pulsonic Ag, Medical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2005
Days to Decision
16 days
Submission Type
Summary

CARDIOSCOPE SONOPLUS 3000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051126
510(k) Type
Traditional
Applicant
Pulsonic Ag, Medical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2005
Days to Decision
16 days
Submission Type
Summary