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 | Device Class | Medical Specialty |
|---|---|---|---|
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified | FDA class 2 | Radiology |
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Other Clearances by Canon USA, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K090623 | DIGITAL RADIOGRAPHY CXDI-40G COMPACT | Mar 24, 2009 | Substantially Equivalent |
| K033624 | PACS SOFTWARE SOLUTION 2003 | Dec 15, 2003 | Substantially Equivalent |
| K031633 | CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C | Jun 11, 2003 | Substantially Equivalent |
| K031629 | CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI | Jun 6, 2003 | Substantially Equivalent |
| K023750 | CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G | Nov 22, 2002 | Substantially Equivalent |
| K023586 | DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS | Nov 5, 2002 | Substantially Equivalent |
| K003689 | CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31 | Jan 2, 2002 | Substantially Equivalent |
| K992606 | CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 | Jun 21, 2000 | Substantially Equivalent |
| K992547 | CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22 | Oct 13, 1999 | Substantially Equivalent |
| K981556 | CANON X-RAY DIGITAL CAMERA CXDI-11 | Nov 4, 1998 | Substantially Equivalent |