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LEUKO EZ VUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071712
510(k) Type
Traditional
Applicant
TECHLAB INC., CORPORATE RESEARCH CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2007
Days to Decision
165 days
Submission Type
Summary

LEUKO EZ VUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071712
510(k) Type
Traditional
Applicant
TECHLAB INC., CORPORATE RESEARCH CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2007
Days to Decision
165 days
Submission Type
Summary