Oncolog Medical QA AB
SwedenFDA applicant, unverified
- Devices
- 2
What Oncolog Medical QA AB makes
Oncolog Medical QA AB manufactures the PATLOG 2.0 and PATLOG Patient Handling System, including the PATLOG Toplog Table Top (models 1.0 and 1.0C). These devices are designed for patient positioning and support in radiation therapy and imaging procedures, ensuring precise alignment and stability during treatment.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is authorised for use in the United States, where the manufacturer is based.
Catalogue
Patlog 2.0 Ref K092939
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oncolog Medical QA AB have in the registry?
The registry currently lists 2 devices for Oncolog Medical QA AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oncolog Medical QA AB's devices?
Among its 2 most recently registered devices, Oncolog Medical QA AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Oncolog Medical QA AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oncolog Medical QA AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oncolog Medical QA AB in the registry?
The most recently registered devices listed for Oncolog Medical QA AB include PATLOG 2.0 and PATLOG, PATLOG PATIENT HANDLING SYSTEM, PATLOG TOPLOG TABLE TOP, MODEL(S) 1.0, 1.0, C.