Automata, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Automata, Inc. makes
Automata, Inc. manufactures medical devices for measuring temperature and conductivity, including the NEO-I Temperature & Conductivity Meter and its modified variant. These devices are designed for clinical and laboratory use to monitor and record precise environmental or sample parameters.
The company’s portfolio is regulated as Class II devices under FDA requirements, with products authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, and the company operates from the United States.
Catalogue
Neo-I Temperature & Conductivity Meter Ref K871708
Regimes: 510(k) Registry: 510(k)Modified Neo-I Temperature, Conductivity Meter Ref K881098
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Automata, Inc. have in the registry?
The registry currently lists 2 devices for Automata, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Automata, Inc.'s devices?
Among its 2 most recently registered devices, Automata, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Automata, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Automata, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Automata, Inc. in the registry?
The most recently registered devices listed for Automata, Inc. include NEO-I TEMPERATURE & CONDUCTIVITY METER and MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER.