FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DAR-9400F
K Number: K072006
·
Decision Aug 31, 2007
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
198
Applicant Total
49
Review Days
39
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Basic Information
- Device Name
- DAR-9400F
- K Number
- K072006
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 892.1600
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Shimadzu Corp.
- Date Received
- July 23, 2007
- Decision Date
- August 31, 2007
- Product Code
- IZI
- 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 |
|---|---|---|---|
| IZI | System, X-Ray, Angiographic | FDA class 2 | Radiology |
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