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IPS E.MAX PRESS MULTI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120134
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2012
Days to Decision
160 days
Submission Type
Statement

IPS E.MAX PRESS MULTI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120134
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2012
Days to Decision
160 days
Submission Type
Statement