FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
IGUIDE SYSTEM
K Number: K062611
·
Decision Sep 20, 2006
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
3
Review Days
15
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Basic Information
- Device Name
- IGUIDE SYSTEM
- K Number
- K062611
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medical Intelligence Medizintechnik-GmbH-An Elekta
- Date Received
- September 5, 2006
- Decision Date
- September 20, 2006
- Product Code
- IYE
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| IYE | Accelerator, Linear, Medical | FDA class 2 | Radiology |
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