Last synced on 27 January 2023 at 11:04 pm

VISTITOME 20-10 MICROKERATOME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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