FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INTRAX FILM PROCESSOR
K Number: K093503
·
Decision Jan 6, 2010
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
82
Applicant Total
3
Review Days
55
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Basic Information
- Device Name
- INTRAX FILM PROCESSOR
- K Number
- K093503
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1900
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Velopex International, Inc.
- Date Received
- November 12, 2009
- Decision Date
- January 6, 2010
- Product Code
- IXW
- 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 |
|---|---|---|---|
| IXW | Processor, Radiographic-Film, Automatic | FDA class 2 | Radiology |
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