RYDER CONTACT LENS CASE MODEL 10670

RYDER CONTACT LENS CASE MODEL 10670 is an FDA 510(k)-cleared medical device (K951182) manufactured by Bradstreet Clinical Research Assoc., Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 15, 1995. Regulation: 8.