
Richard Wolf Medical Instruments Corp.
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CO2 LASER BRONCHOSCOPE SYSTEM is an FDA 510(k)-cleared medical device (K861583) manufactured by Richard Wolf Medical Instruments Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 1986. Regulation: 8.

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