
Jack Speer and Assoc., Inc.
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JSA REPROCESSED COMPRESSION SLEEVE DEVICES is an FDA 510(k)-cleared medical device (K031722) manufactured by Jack Speer and Assoc., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 2003. Regulation: 8.