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INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911116
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1991
Days to Decision
288 days

INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911116
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1991
Days to Decision
288 days