Braemar, Inc.
BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER
SKU K072008UPC DRG
In Stock
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IIFDA 510(k) Cleared (K072008)
1
Free shipping on orders over $99 · 30-day returns
Braemar, Inc.
Free shipping on orders over $99 · 30-day returns
BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER is an FDA 510(k)-cleared medical device (K072008) manufactured by Braemar, 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 October 2, 2007. Regulation: 8.
