FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
K Number: K130377
·
Decision May 17, 2013
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
9
Review Days
92
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Basic Information
- Device Name
- KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
- K Number
- K130377
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 892.1680
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medicatech USA
- Date Received
- February 14, 2013
- Decision Date
- May 17, 2013
- Product Code
- MQB
- 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 |
|---|---|---|---|
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) | FDA class 2 | Radiology |
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