Richmann Laboratories
Country not established
- Devices
- 1
What Richmann Laboratories makes
Richmann Laboratories manufactures the RE-VENT Arterial Blood Sampler and/or Biosampler, a device designed for collecting arterial blood samples in clinical or research settings.
The company’s portfolio includes Class II devices, authorised via the FDA’s 510(k) pathway. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Re-Vent Arterial Blood Sampler And/Or Biosampler Ref K882975
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Richmann Laboratories have in the registry?
The registry currently lists 1 device for Richmann Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Richmann Laboratories's devices?
Among its 1 most recently registered device, Richmann Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Richmann Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Richmann Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Richmann Laboratories in the registry?
The most recently registered devices listed for Richmann Laboratories include RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER.