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INTRALASE 600C LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K993153
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
87 days
Submission Type
Summary

INTRALASE 600C LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K993153
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
87 days
Submission Type
Summary