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IRIS OCULIGHT SL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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