
Innervision, Inc.
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INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES is an FDA 510(k)-cleared medical device (K940731) manufactured by Innervision, 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 September 12, 1994. Regulation: 8.