FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C

K Number: K031633 · Decision Jun 11, 2003
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
48
Review Days
15

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Basic Information

Device Name
CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
K Number
K031633
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon USA, Inc.
Date Received
May 27, 2003
Decision Date
June 11, 2003
Product Code
MQB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQB), ordered by most recent decision date.

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Other Clearances by Canon USA, Inc.

K Number Device Name
K090623 DIGITAL RADIOGRAPHY CXDI-40G COMPACT
K033624 PACS SOFTWARE SOLUTION 2003
K031629 CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
K023750 CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G
K023586 DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS
K003689 CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31
K992606 CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100
K992547 CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22
K981556 CANON X-RAY DIGITAL CAMERA CXDI-11
K980246 NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM
Search all 48 clearances from Canon USA, Inc. →