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TERATECH MODEL 2000 HANDHELD ULTRASOUND SYSTEM WITH DOPPLER AND HARMONIC IMAGING MODES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012191
510(k) Type
Traditional
Applicant
Teratech Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2001
Days to Decision
13 days
Submission Type
Summary

TERATECH MODEL 2000 HANDHELD ULTRASOUND SYSTEM WITH DOPPLER AND HARMONIC IMAGING MODES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012191
510(k) Type
Traditional
Applicant
Teratech Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2001
Days to Decision
13 days
Submission Type
Summary