FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
Uroview FD
K Number: K161019
·
Decision Aug 17, 2016
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
3
Review Days
127
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Basic Information
- Device Name
- Uroview FD
- K Number
- K161019
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pausch Medical GmbH
- Date Received
- April 12, 2016
- Decision Date
- August 17, 2016
- Product Code
- JAA
- 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 |
|---|---|---|---|
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified | FDA class 2 | Radiology |
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