Parkell, Inc.
GENTAL PULSE
SKU K950238UPC EAT
In Stock
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IIFDA 510(k) Cleared (K950238)
1
Free shipping on orders over $99 · 30-day returns
Parkell, Inc.
Free shipping on orders over $99 · 30-day returns
GENTAL PULSE is an FDA 510(k)-cleared medical device (K950238) manufactured by Parkell, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 1995. Regulation: 8.
