Palaistra Systems, Inc.
THE HERMES SYSTEM
SKU K050929UPC DRG
In Stock
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IIFDA 510(k) Cleared (K050929)
1
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Palaistra Systems, Inc.
Free shipping on orders over $99 · 30-day returns
THE HERMES SYSTEM is an FDA 510(k)-cleared medical device (K050929) manufactured by Palaistra Systems, 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 19, 2005. Regulation: 8.
