Technicon Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Technicon Corp. makes
Technicon Corp. manufactures electronic fever thermometers, including the Technion model, designed for rapid and precise body temperature measurement. The company also produces the RA 1000 system, a laboratory analyzer used for automated blood analysis, including hematology and coagulation testing.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. The portfolio is listed in the FDA’s 510(k) registry. Technicon Corp. is headquartered in the United States.
Catalogue
Technion Electronic Fever Thermometer Ref K791323
Regimes: 510(k) Registry: 510(k)Technicon Ra 1000 System Ref K813077
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technicon Corp. have in the registry?
The registry currently lists 2 devices for Technicon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technicon Corp.'s devices?
Among its 2 most recently registered devices, Technicon Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Technicon Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Technicon Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technicon Corp. in the registry?
The most recently registered devices listed for Technicon Corp. include TECHNION ELECTRONIC FEVER THERMOMETER and TECHNICON RA 1000 SYSTEM.