Laboratory Equipment Design Co.
Country not established
- Devices
- 1
What Laboratory Equipment Design Co. makes
Laboratory Equipment Design Co. manufactures a cystic fibrosis testing instrument designed for diagnostic use in clinical laboratories. The device facilitates genetic analysis to detect mutations associated with cystic fibrosis, supporting early and accurate patient diagnosis.
The cystic fibrosis testing instrument 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
Cystic Fibrosis Testing Instrument Ref K772176
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratory Equipment Design Co. have in the registry?
The registry currently lists 1 device for Laboratory Equipment Design Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratory Equipment Design Co.'s devices?
Among its 1 most recently registered device, Laboratory Equipment Design Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Laboratory Equipment Design Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Laboratory Equipment Design Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Laboratory Equipment Design Co. in the registry?
The most recently registered devices listed for Laboratory Equipment Design Co. include CYSTIC FIBROSIS TESTING INSTRUMENT.