FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MIGUE
K Number: K052212
·
Decision Mar 10, 2006
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
22
Review Days
207
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Basic Information
- Device Name
- MIGUE
- K Number
- K052212
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Direx Systems Corp.
- Date Received
- August 15, 2005
- Decision Date
- March 10, 2006
- Product Code
- IYE
- 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 |
|---|---|---|---|
| IYE | Accelerator, Linear, Medical | FDA class 2 | Radiology |
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| K061713 | MAGIS1;MAGIS2 | Jul 21, 2006 | Substantially Equivalent |
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