Comparison of Two Soft Bifocal Contact Lenses

Inclusion Criteria: * The subject must between 35 and 70 years of age. * The subject must have presbyopic symptoms or be already wearing presbyopic contact lens correction. * The subject's spherical equivalent distance refraction must be in the range of -1.00 to -6.00 or -9.00 to -10.00 in each eye. * Refractive cylinder must be -0.75 D in each eye. * The subject must have an ADD power of +0.75D to +2.50D in each eye. * The subject must have best corrected visual acuity of 20/20-3 or better in each eye * The subject's must have at least 20/30-distance vision OU with the study contact lenses. * The subject must agree that they are comfortable with their vision prior to being dispensed the study lenses * The subject must be an adapted soft contact lens wearer in both eyes. * The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol. * The subject must read and sign the STATEMENT OF INFORMED CONSENT and be provided a copy of the form. Exclusion Criteria: * Ocular or systemic allergies or disease that may interfere with contact lens wear. * Systemic disease, autoimmune disease or use of medication, which may interfere with contact lens wear. * Clinically significant (grade 3 or 4) corneal edema, corneal vascularization, corneal staining or any other abnormality of the cornea, which may contraindicate contact lens wear * Clinically significant (grade 3 or 4) tarsal abnormalities that might interfere with contact lens wear. * Any ocular infection. * Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear. * Pregnancy or lactation * Any infectious disease (e.g., hepatitis, tuberculosis) or an immunosuppressive disease (e.g., HIV). * History of diabetes * History of binocular vision abnormality or strabismus