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IRIS OCULIGHT(R) SLX

Page Type
Cleared 510(K)
510(k) Number
K913430
510(k) Type
Traditional
Applicant
IRIDERM DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/1991
Days to Decision
106 days
Submission Type
Statement

IRIS OCULIGHT(R) SLX

Page Type
Cleared 510(K)
510(k) Number
K913430
510(k) Type
Traditional
Applicant
IRIDERM DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/1991
Days to Decision
106 days
Submission Type
Statement