
Spectro Industries, Inc.
Free shipping on orders over $99 · 30-day returns
KANIEVSKI SENSORY AID OR DEVICE is an FDA 510(k)-cleared medical device (K843433) manufactured by Spectro Industries, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on November 13, 1984.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031