Feliks Plastik Laminasyon VE Ambalaj Malzemeleri
TürkiyeFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bodygard SFS Surgical Gown Level 4 Ref K221139
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Feliks Plastik Laminasyon VE Ambalaj Malzemeleri have in the registry?
The registry currently lists 1 device for Feliks Plastik Laminasyon VE Ambalaj Malzemeleri. Devices recorded under merged duplicate company entries are counted once.
Which registries list Feliks Plastik Laminasyon VE Ambalaj Malzemeleri's devices?
Among its 1 most recently registered device, Feliks Plastik Laminasyon VE Ambalaj Malzemeleri has devices listed in FDA 510(k) (1 device).
What risk classes do Feliks Plastik Laminasyon VE Ambalaj Malzemeleri's devices fall under?
Among its 1 most recently registered device, the classes recorded for Feliks Plastik Laminasyon VE Ambalaj Malzemeleri's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Feliks Plastik Laminasyon VE Ambalaj Malzemeleri in the registry?
The most recently registered devices listed for Feliks Plastik Laminasyon VE Ambalaj Malzemeleri include Bodygard SFS Surgical Gown Level 4.