
Bausch & Lomb, Inc.
Free shipping on orders over $99 · 30-day returns
SOUNDCHOICE K-AMP is an FDA 510(k)-cleared medical device (K923735) manufactured by Bausch & Lomb, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 27, 1992. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031