510(k) K072357

NEWTOM VG COMPUTED TOMOGRAPHY X-RAY SYSTEM by Afp Imaging Corp. — Product Code MUH

K072357 is an FDA 510(k) premarket notification submitted by Afp Imaging Corp. for the device "NEWTOM VG COMPUTED TOMOGRAPHY X-RAY SYSTEM". The FDA issued a decision of Substantially Equivalent on September 18, 2007. The device falls under product code MUH (System, X-Ray, Extraoral Source, Digital), a Class II device regulated under 21 CFR 872.1800. Afp Imaging Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 2007
Date Received
August 22, 2007
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Extraoral Source, Digital
Device Class
Class II
Regulation Number
872.1800
Review Panel
RA
Submission Type