Paceart, Inc.
PACEART TX3 CARDIAC EVENT RECORDER
SKU K012407UPC DXH
In Stock
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IIFDA 510(k) Cleared (K012407)
1
Free shipping on orders over $99 · 30-day returns
Paceart, Inc.
Free shipping on orders over $99 · 30-day returns
PACEART TX3 CARDIAC EVENT RECORDER is an FDA 510(k)-cleared medical device (K012407) manufactured by Paceart, 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 August 13, 2001. Regulation: 8.
