Whittaker General Medical
Country not established
- Devices
- 1
What Whittaker General Medical makes
Whittaker General Medical manufactures a combined centrifuge device for performing hematocrit and micro-sedimentation tests, enabling simultaneous blood analysis and sediment examination in clinical or laboratory settings.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Whittaker General Medical have in the registry?
The registry currently lists 1 device for Whittaker General Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whittaker General Medical's devices?
Among its 1 most recently registered device, Whittaker General Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Whittaker General Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Whittaker General Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whittaker General Medical in the registry?
The most recently registered devices listed for Whittaker General Medical include CENTIFUGE, HEMATOCRIT & MICROSEDIMENTATION COMBINE.