Radiation-Emitting Products

We are adding an FFDM unit to our already certified digital facility. We know that we have to perform an MEE on the unit prior to clinical use. However, since our review workstation and laser printer (accessory components) have already undergone an MEE and are currently being used with our first unit, do they have to undergo a new MEE or can we use their original MEE or a subsequent annual ph...

Policy Guidance Help System logo

Same answer as in Question 11.

Back to Other Modalities Quality Control Tests

Page Last Updated: 08/11/2014
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English