KARL STORZ PUNCTURE, INJECTION, ENDOSCOPIC, VERESS NEEDLE

KARL STORZ PUNCTURE, INJECTION, ENDOSCOPIC, VERESS NEEDLE is an FDA 510(k)-cleared medical device (K951190) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 13, 1995. Regulation: 8.