
ETHICON, Inc.
Free shipping on orders over $99 · 30-day returns
E-PACK PROCEDURE KITS is an FDA 510(k)-cleared medical device (K951476) manufactured by ETHICON, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 1995. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031