Last synced on 13 June 2025 at 11:06 pm

VARIOLINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931309
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
129 days
Submission Type
Statement

VARIOLINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931309
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
129 days
Submission Type
Statement