PAROJECT ANESTHETIC SYRINGE

PAROJECT ANESTHETIC SYRINGE is an FDA 510(k)-cleared medical device (K904279) manufactured by Ronvig Instruments, 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 December 6, 1990. Regulation: 8.