FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS
K Number: K093581
·
Decision Apr 19, 2011
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
61
Review Days
517
Basic Information
- Device Name
- DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS
- K Number
- K093581
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1750
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- GE MEDICAL SYSTEMS, LLC
- Date Received
- November 18, 2009
- Decision Date
- April 19, 2011
- Product Code
- JAK
- 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 |
|---|---|---|---|
| JAK | System, X-Ray, Tomography, Computed | FDA class 2 | Radiology |
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