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OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE

Page Type
Cleared 510(K)
510(k) Number
K982031
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1998
Days to Decision
90 days
Submission Type
Summary

OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE

Page Type
Cleared 510(K)
510(k) Number
K982031
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1998
Days to Decision
90 days
Submission Type
Summary