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7.5 MHZ ENDOVAGINAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K870709
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
35 days

7.5 MHZ ENDOVAGINAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K870709
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
35 days