Unimetrics Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Unimetrics Corp. makes
Unimetrics Corp. manufactures heavy glass-wall injection tubes and three-port luer connectors, designed for medical fluid administration and compatibility with infusion systems.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Tube, Heavy Glass Wall Injection Ref K760500
Regimes: 510(k) Registry: 510(k)3 Port Luer Ref K770500
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unimetrics Corp. have in the registry?
The registry currently lists 2 devices for Unimetrics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unimetrics Corp.'s devices?
Among its 2 most recently registered devices, Unimetrics Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Unimetrics Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Unimetrics Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Unimetrics Corp. in the registry?
The most recently registered devices listed for Unimetrics Corp. include TUBE, HEAVY GLASS WALL INJECTION and 3 PORT LUER.