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7.5 MHZ ENDORECTAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K881028
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/1988
Days to Decision
48 days

7.5 MHZ ENDORECTAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K881028
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/1988
Days to Decision
48 days