FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMS
K Number: K082243
·
Decision Nov 7, 2008
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
7
Review Days
92
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Basic Information
- Device Name
- PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMS
- K Number
- K082243
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- General Medical Merate S.P.A
- Date Received
- August 7, 2008
- Decision Date
- November 7, 2008
- Product Code
- OWB
- 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 |
|---|---|---|---|
| OWB | Interventional Fluoroscopic X-Ray System | FDA class 2 | Radiology |
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