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TERASON T3200 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110020
510(k) Type
Traditional
Applicant
TERATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2011
Days to Decision
17 days
Submission Type
Summary

TERASON T3200 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110020
510(k) Type
Traditional
Applicant
TERATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2011
Days to Decision
17 days
Submission Type
Summary