Astral Medical Systems
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Apollo Densitometer Ref K853734
Regimes: 510(k) Registry: 510(k)Modified Coatron Ii And Coatron Jr. Ref K900506
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Astral Medical Systems have in the registry?
The registry currently lists 4 devices for Astral Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Astral Medical Systems's devices?
Among its 4 most recently registered devices, Astral Medical Systems has devices listed in FDA 510(k) (4 devices).
What risk classes do Astral Medical Systems's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Astral Medical Systems's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Astral Medical Systems in the registry?
The most recently registered devices listed for Astral Medical Systems include APOLLO DENSITOMETER, MODIFIED COATRON II AND COATRON JR., ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160, 18 and COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGE.