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VISION DIAGNOSTIC ULTRASONIC SCANNER

Page Type
Cleared 510(K)
510(k) Number
K901467
510(k) Type
Traditional
Applicant
THE PROBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1990
Days to Decision
160 days

VISION DIAGNOSTIC ULTRASONIC SCANNER

Page Type
Cleared 510(K)
510(k) Number
K901467
510(k) Type
Traditional
Applicant
THE PROBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1990
Days to Decision
160 days