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MICROKERATOME, MODEL MK-2000

Page Type
Cleared 510(K)
510(k) Number
K990900
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/1999
Days to Decision
190 days
Submission Type
Summary

MICROKERATOME, MODEL MK-2000

Page Type
Cleared 510(K)
510(k) Number
K990900
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/1999
Days to Decision
190 days
Submission Type
Summary