
Cranston Ind., Inc.
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USI BASIC. AG 1050. AG 1090 is an FDA 510(k)-cleared medical device (K873146) manufactured by Cranston Ind., Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 26, 1987. Regulation: 8.