LEUKO EZ VUE— 510(k) K071712

Substantially Equivalent

Techlab Inc., Corporate Research Center

FDA 510(k) clearance K071712 for LEUKO EZ VUE, Substantially Equivalent on 2007-12-04. Applicant: Techlab Inc., Corporate Research Center.

Clearance details

Applicant: Techlab Inc., Corporate Research Center
Product code: Code DEG
Advisory panel: Immunology
Date received: 2007-06-22
Decision date: 2007-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Blacksburg, VA, US

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