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DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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