KESTREL LENS CASE 1543-893S/P-1700-2611

KESTREL LENS CASE 1543-893S/P-1700-2611 is an FDA 510(k)-cleared medical device (K900054) 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 January 29, 1990. Regulation: 8.