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VERSALUX

Page Type
Cleared 510(K)
510(k) Number
K010133
510(k) Type
Traditional
Applicant
CENTRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2001
Days to Decision
78 days
Submission Type
Statement

VERSALUX

Page Type
Cleared 510(K)
510(k) Number
K010133
510(k) Type
Traditional
Applicant
CENTRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2001
Days to Decision
78 days
Submission Type
Statement