510(k) K103038

DUET DRF by Cmt Medical Technologies, Ltd. — Product Code JAA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 2011
Date Received
October 14, 2010
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Fluoroscopic, Image-Intensified
Device Class
Class II
Regulation Number
892.1650
Review Panel
RA
Submission Type