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DIASONICS 3.5 GWA 30MM PROBE

Page Type
Cleared 510(K)
510(k) Number
K860361
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1986
Days to Decision
117 days

DIASONICS 3.5 GWA 30MM PROBE

Page Type
Cleared 510(K)
510(k) Number
K860361
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1986
Days to Decision
117 days