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IRIS OCULIGHT SL

Page Type
Cleared 510(K)
510(k) Number
K922663
510(k) Type
Traditional
Applicant
IRIDERM DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1992
Days to Decision
82 days
Submission Type
Statement

IRIS OCULIGHT SL

Page Type
Cleared 510(K)
510(k) Number
K922663
510(k) Type
Traditional
Applicant
IRIDERM DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1992
Days to Decision
82 days
Submission Type
Statement