Airspec, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Airspec, Ltd. makes
Airspec, Ltd. manufactures the MGA 2000 Gas Analyser, a device designed for measuring and analysing gas concentrations in medical and industrial environments.
The MGA 2000 Gas Analyser is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mga 2000 Gas Analyser Ref K854076
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airspec, Ltd. have in the registry?
The registry currently lists 1 device for Airspec, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airspec, Ltd.'s devices?
Among its 1 most recently registered device, Airspec, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Airspec, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Airspec, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Airspec, Ltd. in the registry?
The most recently registered devices listed for Airspec, Ltd. include MGA 2000 GAS ANALYSER.