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OPTILUX 501

Page Type
Cleared 510(K)
510(k) Number
K020091
510(k) Type
Traditional
Applicant
KERR CORPORATION (DANBURY)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
70 days
Submission Type
Summary

OPTILUX 501

Page Type
Cleared 510(K)
510(k) Number
K020091
510(k) Type
Traditional
Applicant
KERR CORPORATION (DANBURY)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
70 days
Submission Type
Summary