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DIO-LIGHT LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980201
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1998
Days to Decision
55 days
Submission Type
Summary

DIO-LIGHT LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980201
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1998
Days to Decision
55 days
Submission Type
Summary