FULL SPECTRUM ULE-OVERCLAD FIBER: MODEL 201

FULL SPECTRUM ULE-OVERCLAD FIBER: MODEL 201 is an FDA 510(k)-cleared medical device (K955862) manufactured by Full Spectrum, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 29, 1996. Regulation: 8.