
Aesculap, Inc.
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Aesculap Video Assisted Thoracic Surgery (VATS) INstruments is an FDA 510(k)-cleared medical device (K170683) manufactured by Aesculap, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 19, 2018. Regulation: 8.