Lumac
Country not established
- Devices
- 1
What Lumac makes
Lumac manufactures the Bacteriuria Screening Kit, a diagnostic device designed to detect bacteriuria in urine samples for clinical evaluation.
The Bacteriuria Screening Kit is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lumac's Bacteriuria Screening Kit Ref K810746
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lumac have in the registry?
The registry currently lists 1 device for Lumac. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lumac's devices?
Among its 1 most recently registered device, Lumac has devices listed in FDA 510(k) (1 device).
What risk classes do Lumac's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lumac's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lumac in the registry?
The most recently registered devices listed for Lumac include LUMAC'S BACTERIURIA SCREENING KIT.