LEUKO EZ VUE— 510(k) K071712
Substantially EquivalentTechlab 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. Device class: 1.
Clearance details
- Applicant
- Techlab Inc., Corporate Research Center
- Product code
- Code DEG
- Device class
- Class 1
- Regulation
- 21 CFR 866.5570
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Blacksburg, VA, US
Recent devices under product code DEG
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