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SCALETRON PIEZO ULTRASOUND SCALER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033120
510(k) Type
Traditional
Applicant
Pac-Dent International (Suzhou), Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2004
Days to Decision
121 days
Submission Type
Summary

SCALETRON PIEZO ULTRASOUND SCALER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033120
510(k) Type
Traditional
Applicant
Pac-Dent International (Suzhou), Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2004
Days to Decision
121 days
Submission Type
Summary