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ULTRASHAPER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K990227
510(k) Type
Traditional
Applicant
LASERSIGHT TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2000
Days to Decision
371 days
Submission Type
Summary

ULTRASHAPER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K990227
510(k) Type
Traditional
Applicant
LASERSIGHT TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2000
Days to Decision
371 days
Submission Type
Summary