510(k) K992547

CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22 by Canon USA, Inc. — Product Code MQB

K992547 is an FDA 510(k) premarket notification submitted by Canon USA, Inc. for the device "CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22". The FDA issued a decision of Substantially Equivalent on October 13, 1999. The device falls under product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)), a Class II device regulated under 21 CFR 892.1680. Canon USA, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 13, 1999
Date Received
July 30, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Solid State X-Ray Imager (Flat Panel/Digital Imager)
Device Class
Class II
Regulation Number
892.1680
Review Panel
RA
Submission Type