5012 PARABOLIC STIMULATOR

5012 PARABOLIC STIMULATOR is an FDA 510(k)-cleared medical device (K822923) manufactured by Life-Tech Intl., 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 December 27, 1982. Regulation: 8.