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VISTITOME 20-10 MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K014000
510(k) Type
Traditional
Applicant
BIOVISION AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2002
Days to Decision
97 days
Submission Type
Summary

VISTITOME 20-10 MICROKERATOME

Page Type
Cleared 510(K)
510(k) Number
K014000
510(k) Type
Traditional
Applicant
BIOVISION AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2002
Days to Decision
97 days
Submission Type
Summary