
Jack Speer and Assoc., Inc.
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JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES is an FDA 510(k)-cleared medical device (K040065) 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 March 28, 2004. Regulation: 8.