REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT

REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT is an FDA 510(k)-cleared medical device (K130282) manufactured by Remington Medical, 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 May 12, 2013. Regulation: 8.