Last synced on 25 April 2025 at 11:05 pm

EOS INLAY MATERIAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896469
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1990
Days to Decision
193 days

EOS INLAY MATERIAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896469
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1990
Days to Decision
193 days