Regional Media Laboratories
Country not established
- Devices
- 2
What Regional Media Laboratories makes
Regional Media Laboratories produces microbiological culture media, including CAMPY Blood Agar and Haemophilus Test Medium (broth), used for isolating and identifying specific bacteria in clinical and diagnostic settings.
These products are regulated under FDA’s 510(k) pathway, with some classified as Class I and others as Class II devices. They are listed in the FDA’s 510(k) database and are manufactured in the United States.
Catalogue
Campy Blood Agar Ref K792674
Regimes: 510(k) Registry: 510(k)Haemophilus Test Medium (Broth) Ref K894848
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regional Media Laboratories have in the registry?
The registry currently lists 2 devices for Regional Media Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regional Media Laboratories's devices?
Among its 2 most recently registered devices, Regional Media Laboratories has devices listed in FDA 510(k) (2 devices).
What risk classes do Regional Media Laboratories's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Regional Media Laboratories's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Regional Media Laboratories in the registry?
The most recently registered devices listed for Regional Media Laboratories include CAMPY BLOOD AGAR and HAEMOPHILUS TEST MEDIUM (BROTH).