
Richard Wolf Medical Instruments Corp.
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MODEL 5135 AUTO LP/FLASH is an FDA 510(k)-cleared medical device (K944607) manufactured by Richard Wolf Medical Instruments Corp.. 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 December 12, 1994. Regulation: 8.