
J & S Medical Assoc., Inc.
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EYE SPOT RF TEST is an FDA 510(k)-cleared medical device (K932437) manufactured by J & S Medical Assoc., Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 22, 1993. Regulation: 8.