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TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS

Page Type
Cleared 510(K)
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)
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