ERBE BICLAMP OPEN AND LAPAROSCOPIC INSTRUMENTS

ERBE BICLAMP OPEN AND LAPAROSCOPIC INSTRUMENTS is an FDA 510(k)-cleared medical device (K060170) manufactured by Erbe USA, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 15, 2006. Regulation: 8.