FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
OCTAVIUS I, OCTAVIUS II, OCTAVIUS III, OCTAVIUS 4D
K Number: K160405
·
Decision Oct 20, 2017
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
3
Review Days
612
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- OCTAVIUS I, OCTAVIUS II, OCTAVIUS III, OCTAVIUS 4D
- K Number
- K160405
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ptw-Freiburg Physikalisch-Technische-Werkstaetten
- Date Received
- February 16, 2016
- Decision Date
- October 20, 2017
- Product Code
- IYE
- 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 |
|---|---|---|---|
| IYE | Accelerator, Linear, Medical | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IYE), ordered by most recent decision date.
ThinkQA 3
FDA 510(k)
FDA Class 2
·Radiology
LUNA 3D
FDA 510(k)
FDA Class 2
·Radiology
AerFrame Patient Immobilization System (AFPIS)
FDA 510(k)
FDA Class 2
·Radiology
VERIQA RT EPID 3D
FDA 510(k)
FDA Class 2
·Radiology
ClearCheck (RADCC V2.7)
FDA 510(k)
FDA Class 2
·Radiology
AlignRT Plus (8.0)
FDA 510(k)
FDA Class 2
·Radiology