
Minnesota Laser Corp.
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FOR USE IN EAR; NOSE & THROAT MICROSURGERY is an FDA 510(k)-cleared medical device (K852695) manufactured by Minnesota Laser Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 29, 1985. Regulation: 8.

Ansell
SKU MSC846624

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SKU VM-1270030

Hollister
SKU VM-1270031