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

CANON X-RAY IMAGE DISTRIBUTOR

K Number: K853984 · Decision Oct 16, 1985
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
48
Review Days
19

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Basic Information

Device Name
CANON X-RAY IMAGE DISTRIBUTOR
K Number
K853984
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Canon USA, Inc.
Date Received
September 27, 1985
Decision Date
October 16, 1985
Product Code
JAA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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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
K031633 CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
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
Search all 48 clearances from Canon USA, Inc. →