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DIASONICS QT ENDORECTAL 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K880714
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1988
Days to Decision
59 days

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K880714
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1988
Days to Decision
59 days