
Lifestream Int'L, Inc.
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DISPOSABLE SUCTION CANNULA NO. 902008-000 is an FDA 510(k)-cleared medical device (K863293) manufactured by Lifestream Int'L, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 8, 1986. Regulation: 8.