
Polytec Pi, Inc.
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LASEAWAY LONG PULSE AND Q-SWITCHED RUBY LASER SYSTEM is an FDA 510(k)-cleared medical device (K971193) manufactured by Polytec Pi, 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 June 23, 1997. Regulation: 8.