Reprocessed Tri Pulse Compression Garment

Reprocessed Tri Pulse Compression Garment is an FDA 510(k)-cleared medical device (K203847) manufactured by Renu Medical, 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 May 6, 2021. Regulation: 8.