Precision Therapy Intl., Inc.
PRECISEPLAN 2.0
SKU K022411UPC MUJ
In Stock
—
IIFDA 510(k) Cleared (K022411)
1
Free shipping on orders over $99 · 30-day returns
Precision Therapy Intl., Inc.
Free shipping on orders over $99 · 30-day returns
PRECISEPLAN 2.0 is an FDA 510(k)-cleared medical device (K022411) manufactured by Precision Therapy Intl., Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 2002. Regulation: 8.
