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DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K864908
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
102 days

DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K864908
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
102 days