Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim
TürkiyeFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Fiberion Ophthalmic Endolaser Probe Ref K133019
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim have in the registry?
The registry currently lists 1 device for Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim's devices?
Among its 1 most recently registered device, Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim has devices listed in FDA 510(k) (1 device).
What risk classes do Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim's devices fall under?
Among its 1 most recently registered device, the classes recorded for Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim in the registry?
The most recently registered devices listed for Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim include FIBERION OPHTHALMIC ENDOLASER PROBE.