FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AGFA DIAGNOSTIC CENTER (ADC)
K Number: K904519
·
Decision Jun 21, 1991
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
4
Review Days
261
Basic Information
- Device Name
- AGFA DIAGNOSTIC CENTER (ADC)
- K Number
- K904519
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- ENHANCED IMAGING TECHNOLOGIES, INC.
- Date Received
- October 3, 1990
- Decision Date
- June 21, 1991
- Product Code
- LLZ
- 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 |
|---|---|---|---|
| LLZ | System, Image Processing, Radiological | FDA class 2 | Radiology |
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