KESTREL LENS CASE (208-12NT POLYSTYRENE)

KESTREL LENS CASE (208-12NT POLYSTYRENE) is an FDA 510(k)-cleared medical device (K901748) manufactured by Kestrel. 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 30, 1990. Regulation: 8.