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SSI-8000/S8/S6 DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM, 2P1 PHASED ARRAY DIAGNOSTIC ULTRASOUND TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092922
510(k) Type
Traditional
Applicant
Sonoscape Company Limited
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2010
Days to Decision
170 days
Submission Type
Summary

SSI-8000/S8/S6 DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM, 2P1 PHASED ARRAY DIAGNOSTIC ULTRASOUND TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092922
510(k) Type
Traditional
Applicant
Sonoscape Company Limited
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2010
Days to Decision
170 days
Submission Type
Summary