Arlanda Medicinska Instrument Co. AB
SwedenFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Intracavity Needle Guide Kit Ref K955668
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arlanda Medicinska Instrument Co. AB have in the registry?
The registry currently lists 1 device for Arlanda Medicinska Instrument Co. AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arlanda Medicinska Instrument Co. AB's devices?
Among its 1 most recently registered device, Arlanda Medicinska Instrument Co. AB has devices listed in FDA 510(k) (1 device).
What risk classes do Arlanda Medicinska Instrument Co. AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arlanda Medicinska Instrument Co. AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arlanda Medicinska Instrument Co. AB in the registry?
The most recently registered devices listed for Arlanda Medicinska Instrument Co. AB include INTRACAVITY NEEDLE GUIDE KIT.