PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN)

PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN) is an FDA 510(k)-cleared medical device (K854577) manufactured by Austin Biological Laboratories. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 1986. Regulation: 8.