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TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112953
510(k) Type
Traditional
Applicant
TERATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2012
Days to Decision
122 days
Submission Type
Summary

TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112953
510(k) Type
Traditional
Applicant
TERATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2012
Days to Decision
122 days
Submission Type
Summary