FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
COMPACS, VERSION 1.0
K Number: K041581
·
Decision Jun 22, 2004
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
2
Review Days
8
Basic Information
- Device Name
- COMPACS, VERSION 1.0
- K Number
- K041581
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- INTELLIGENT IMAGES SRL
- Date Received
- June 14, 2004
- Decision Date
- June 22, 2004
- Product Code
- LLZ
- 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 |
|---|---|---|---|
| LLZ | System, Image Processing, Radiological | FDA class 2 | Radiology |
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Other Clearances by INTELLIGENT IMAGES SRL
| K Number | Device Name | ||
|---|---|---|---|
| K022940 | IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 | Oct 11, 2002 | Substantially Equivalent |