Iris
Country not established
- Devices
- 1
What Iris makes
Iris manufactures specific gravity instruments designed for measuring the density of liquids, commonly used in clinical and laboratory settings to assess urine or other bodily fluids.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Specific Gravity Instrument Ref K831213
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iris have in the registry?
The registry currently lists 1 device for Iris. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iris's devices?
Among its 1 most recently registered device, Iris has devices listed in FDA 510(k) (1 device).
What risk classes do Iris's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iris's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Iris in the registry?
The most recently registered devices listed for Iris include SPECIFIC GRAVITY INSTRUMENT.