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SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080089
510(k) Type
Traditional
Applicant
Sybron Dental Specialties, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2008
Days to Decision
234 days
Submission Type
Summary

SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080089
510(k) Type
Traditional
Applicant
Sybron Dental Specialties, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2008
Days to Decision
234 days
Submission Type
Summary