Mti Corp./ Electrostar S.A.-Haiti
DUOSTAR
SKU K974170UPC GEI
In Stock
—
IIFDA 510(k) Cleared (K974170)
1
Free shipping on orders over $99 · 30-day returns
Mti Corp./ Electrostar S.A.-Haiti
Free shipping on orders over $99 · 30-day returns
DUOSTAR is an FDA 510(k)-cleared medical device (K974170) manufactured by Mti Corp./ Electrostar S.A.-Haiti. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 1998. Regulation: 8.
