Quinton, Inc.
Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
SKU K003576UPC DSI
In Stock
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IIFDA 510(k) Cleared (K003576)
1
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Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503 is an FDA 510(k)-cleared medical device (K003576) manufactured by Quinton, 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 January 24, 2001. Regulation: 8.
