Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Creative Plastic Technology
Free shipping on orders over $99 · 30-day returns
MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000 is an FDA 510(k)-cleared medical device (K001106) manufactured by Creative Plastic Technology. 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 August 15, 2000. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

Ohmeda Medical
SKU K871399

Insulet Corporation
SKU K182630