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CARDIOSCOPE SONOPLUS 3000

Page Type
Cleared 510(K)
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)
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