FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600
K Number: K093816
·
Decision Oct 5, 2010
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
3
Review Days
298
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Basic Information
- Device Name
- DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600
- K Number
- K093816
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1680
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medien International Co, Ltd.
- Date Received
- December 11, 2009
- Decision Date
- October 5, 2010
- Product Code
- KPR
- 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 |
|---|---|---|---|
| KPR | System, X-Ray, Stationary | FDA class 2 | Radiology |
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