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SIGMA 110/330 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002239
510(k) Type
Traditional
Applicant
Kontron Medical Systems Sas
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2000
Days to Decision
15 days
Submission Type
Summary

SIGMA 110/330 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002239
510(k) Type
Traditional
Applicant
Kontron Medical Systems Sas
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2000
Days to Decision
15 days
Submission Type
Summary