Persyst Development Corp.
PRESSON ELECTRODE
SKU K103103UPC GXZ
In Stock
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IIFDA 510(k) Cleared (K103103)
1
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Persyst Development Corp.
Free shipping on orders over $99 · 30-day returns
PRESSON ELECTRODE is an FDA 510(k)-cleared medical device (K103103) manufactured by Persyst Development Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 7, 2011. Regulation: 8.
