Devon Medical, Inc.
ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE
SKU K102582UPC JOW
In Stock
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IIFDA 510(k) Cleared (K102582)
1
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Devon Medical, Inc.
Free shipping on orders over $99 · 30-day returns
ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE is an FDA 510(k)-cleared medical device (K102582) manufactured by Devon 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 October 6, 2010. Regulation: 8.
