Nash & Assoc.
Country not established
- Devices
- 1
What Nash & Assoc. makes
Nash & Assoc. manufactures the EARSCOPE, a device designed for otoscopic examinations to visualize the ear canal and tympanic membrane.
The EARSCOPE is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Earscope Ref K800365
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nash & Assoc. have in the registry?
The registry currently lists 1 device for Nash & Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nash & Assoc.'s devices?
Among its 1 most recently registered device, Nash & Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nash & Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nash & Assoc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nash & Assoc. in the registry?
The most recently registered devices listed for Nash & Assoc. include EARSCOPE.