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HORUS LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K062314
510(k) Type
Traditional
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
136 days
Submission Type
Summary

HORUS LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K062314
510(k) Type
Traditional
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
136 days
Submission Type
Summary