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COMBISON 530D WITH POWER DOPPLER MODE

Page Type
Cleared 510(K)
510(k) Number
K974813
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1998
Days to Decision
280 days
Submission Type
Summary

COMBISON 530D WITH POWER DOPPLER MODE

Page Type
Cleared 510(K)
510(k) Number
K974813
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1998
Days to Decision
280 days
Submission Type
Summary