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INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST

Page Type
Cleared 510(K)
510(k) Number
K911117
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1991
Days to Decision
285 days

INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST

Page Type
Cleared 510(K)
510(k) Number
K911117
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1991
Days to Decision
285 days