510(k) K040746

MRA-CMS by Medis Medical Imaging Systems BV — Product Code LLZ

K040746 is an FDA 510(k) premarket notification submitted by Medis Medical Imaging Systems BV for the device "MRA-CMS". The FDA issued a decision of Substantially Equivalent on June 8, 2004. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Medis Medical Imaging Systems BV has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 8, 2004
Date Received
March 23, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type