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ODYSSEY 2.4G, DENLASER ELITE, MODEL 002-00050

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050453
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
94 days
Submission Type
Summary

ODYSSEY 2.4G, DENLASER ELITE, MODEL 002-00050

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050453
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
94 days
Submission Type
Summary