Histo-Med, Inc.
Country not established
- Devices
- 1
What Histo-Med, Inc. makes
Histo-Med, Inc. makes a sickle cell test kit.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Sickle Cell Test Kit Ref K932872
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Histo-Med, Inc. have in the registry?
The registry currently lists 1 device for Histo-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Histo-Med, Inc.'s devices?
Among its 1 most recently registered device, Histo-Med, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Histo-Med, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Histo-Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Histo-Med, Inc. in the registry?
The most recently registered devices listed for Histo-Med, Inc. include SICKLE CELL TEST KIT.