Northland Cataract & Eye Care Clinic
Country not established
- Devices
- 1
What Northland Cataract & Eye Care Clinic makes
Northland Cataract & Eye Care Clinic manufactures the TearTec Rapid Lacrimal Assessment System, a diagnostic device used to evaluate tear film production and dry eye conditions by measuring basal tear secretion rates.
The device is classified as Class I under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The clinic operates in the United States.
Catalogue
Teartec Rapid Lacrimal Assesment System Ref K911734
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Northland Cataract & Eye Care Clinic have in the registry?
The registry currently lists 1 device for Northland Cataract & Eye Care Clinic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Northland Cataract & Eye Care Clinic's devices?
Among its 1 most recently registered device, Northland Cataract & Eye Care Clinic has devices listed in FDA 510(k) (1 device).
What risk classes do Northland Cataract & Eye Care Clinic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Northland Cataract & Eye Care Clinic's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Northland Cataract & Eye Care Clinic in the registry?
The most recently registered devices listed for Northland Cataract & Eye Care Clinic include TEARTEC RAPID LACRIMAL ASSESMENT SYSTEM.