Evaluation of the Performance of Two Contact Lenses Compared to a Marketed Lens

Inclusion Criteria: * Healthy, female adult, at least 18 years of age, and no more than 34 years of age * The subjects must be female, light eye Caucasian, Non-Hispanic, habitual soft contact lens wearer (both eyes) with light or dark eyes * Must have rated the Concept Statement positively (i.e., a rating of 4 or 5). * Optimal vertexed spherical equivalent distance correction must be between -1.00 and -4.00 diopters (D) * Any cylinder power must be: \<=0.75D * Visual acuity must be best correctable to 20/25 or better for each eye * Must have normal eyes (no ocular medications or ocular infection of any type) * Must read and sign the Statement of Informed Consent * Must appear able and willing to adhere to the instructions set forth in this clinical protocol. Exclusion Criteria: * Ocular or systemic allergies or disease which might interfere with contact lens wear * Systemic disease, autoimmune disease, or use of medication which might interfere with contact lens wear * Clinically significant (grade 3 or worse) corneal edema, corneal neovascularization, corneal staining, or any other abnormalities of the cornea which would contraindicate contact lens wear * Clinically significant (grade 3 or 4) tarsal abnormalities or bulbar injection which might interfere with contact lens wear * Any ocular infection * Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear * Any color deficiencies (colorblindness) - to the best of the subject's knowledge * Pregnancy or lactation * Diabetes * Infectious diseases (e.g. hepatitis, tuberculosis) or an immuno-suppressive disease (e.g. HIV) * Habitual contact lens type is toric, multifocal, or is worn as extended wear. * Subject presents with one dark iris color and one light iris color. * Subject has heterochromia iridis (a difference in color between parts of one iris). * The subject must not be an employee or family member of the clinical study site.