Last synced on 14 November 2025 at 11:06 pm

MULTILINK AUTOMIX

Page Type
Cleared 510(K)
510(k) Number
K123397
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
Liechtenstein
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
87 days
Submission Type
Summary

MULTILINK AUTOMIX

Page Type
Cleared 510(K)
510(k) Number
K123397
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
Liechtenstein
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
87 days
Submission Type
Summary