
Fujifilm Medical System U.S.A., Inc.
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Processor VP-7000, Light Source BL-7000 is an FDA 510(k)-cleared medical device (K163675) manufactured by Fujifilm Medical System U.S.A., 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 April 24, 2017. Regulation: 8.