Aerscher Diagnostics
Country not established FDA establishment FEI 1000219815
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Hemaprompt Gastric Ref K031356
510(k) 510(k)Hemaprompt Ref K972763
510(k) 510(k)Hemaprompt Ref K981661
510(k) 510(k)
Company details
- FDA FEI number
- 1000219815
- Address
- 125 Dixon Drive, CHESTERTOWN, MD, 21620
Frequently asked questions
How many devices does AERSCHER DIAGNOSTICS have in the registry?
The registry currently lists 3 devices for AERSCHER DIAGNOSTICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list AERSCHER DIAGNOSTICS's devices?
Among its 3 most recently registered devices, AERSCHER DIAGNOSTICS has devices listed in FDA 510(k) (3 devices).
What risk classes do AERSCHER DIAGNOSTICS's devices fall under?
Among its 3 most recently registered devices, the classes recorded for AERSCHER DIAGNOSTICS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AERSCHER DIAGNOSTICS in the registry?
The most recently registered devices listed for AERSCHER DIAGNOSTICS include HEMAPROMPT GASTRIC and HEMAPROMPT.