CASPAR SCALP CLIP, APPLIER

CASPAR SCALP CLIP, APPLIER is an FDA 510(k)-cleared medical device (K890443) manufactured by Aesculap Instruments Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 14, 1989. Regulation: 8.