Last synced on 25 January 2026 at 3:41 am

X-L (DW228-14A) AND X-LX (DW228-24A)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913070
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1991
Days to Decision
64 days
Submission Type
Statement

X-L (DW228-14A) AND X-LX (DW228-24A)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913070
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1991
Days to Decision
64 days
Submission Type
Statement