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MODIFICATION TO VISITOME 20-10 MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K042083
510(k) Type
Traditional
Applicant
Biovision AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2004
Days to Decision
105 days
Submission Type
Summary

MODIFICATION TO VISITOME 20-10 MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K042083
510(k) Type
Traditional
Applicant
Biovision AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2004
Days to Decision
105 days
Submission Type
Summary