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FEMTEC LASER MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K033354
510(k) Type
Traditional
Applicant
20/10 PERFECT VISION OPTISCHE GERATE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2004
Days to Decision
121 days
Submission Type
Summary

FEMTEC LASER MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K033354
510(k) Type
Traditional
Applicant
20/10 PERFECT VISION OPTISCHE GERATE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2004
Days to Decision
121 days
Submission Type
Summary