
Kj Meditech Co., Ltd.
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KJ SUBMERGED SYSTEM is an FDA 510(k)-cleared medical device (K103810) manufactured by Kj Meditech Co., Ltd.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 2011. Regulation: 8.