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

Oncology Data Systems, Inc.
Free shipping on orders over $99 · 30-day returns
MUCHECK - MONITOR UNIT VALIDATION PROGRAM, MODEL V4.1 is an FDA 510(k)-cleared medical device (K012227) manufactured by Oncology Data Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 2001. Regulation: 8.