Miacom Diagnostics GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Miacom Diagnostics GmbH makes
Miacom Diagnostics GmbH manufactures the hemoFISH Masterpanel, a Class I medical device.
The company is based in the US and its products are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
hemoFISH Masterpanel Ref K150031
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Miacom Diagnostics GmbH have in the registry?
The registry currently lists 1 device for Miacom Diagnostics GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Miacom Diagnostics GmbH's devices?
Among its 1 most recently registered device, Miacom Diagnostics GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Miacom Diagnostics GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Miacom Diagnostics GmbH's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Miacom Diagnostics GmbH in the registry?
The most recently registered devices listed for Miacom Diagnostics GmbH include hemoFISH Masterpanel.