FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
AYCAN WORKSTATION OSIRIX PRO
K Number: K103546
·
Decision Mar 17, 2011
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
3
Review Days
105
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Basic Information
- Device Name
- AYCAN WORKSTATION OSIRIX PRO
- K Number
- K103546
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Aycan Digitalsysteme GmbH
- Date Received
- December 2, 2010
- Decision Date
- March 17, 2011
- 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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