Greenleaf Medical Systems, Inc.
(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM
SKU K884723UPC KQX
In Stock
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IFDA 510(k) Cleared (K884723)
1
Free shipping on orders over $99 · 30-day returns
Greenleaf Medical Systems, Inc.
Free shipping on orders over $99 · 30-day returns
(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM is an FDA 510(k)-cleared medical device (K884723) manufactured by Greenleaf Medical Systems, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 7, 1989. Regulation: 8.
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