Schlosser Alberti Co.
Country not established
- Devices
- 2
What Schlosser Alberti Co. makes
Schlosser Alberti Co. makes the SA/7860 Fetal Heart Monitor (Doppler) and the S/A 7800 Birth Support Chair.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
SA/7860 Fetal Heart Monitor (Doppler) Ref K790951
Regimes: 510(k) Registry: 510(k)S/A 7800 Birth Support Chair Ref K790950
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schlosser Alberti Co. have in the registry?
The registry currently lists 2 devices for Schlosser Alberti Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schlosser Alberti Co.'s devices?
Among its 2 most recently registered devices, Schlosser Alberti Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Schlosser Alberti Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Schlosser Alberti Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schlosser Alberti Co. in the registry?
The most recently registered devices listed for Schlosser Alberti Co. include SA/7860 FETAL HEART MONITOR (DOPPLER) and S/A 7800 BIRTH SUPPORT CHAIR.