Neutech Corp.
Country not established
- Devices
- 1
What Neutech Corp. makes
Neutech Corp. manufactures the NEUSTEIN LARYNGOSCOPE, a device used for visualizing the larynx during medical procedures such as intubation or airway assessment.
The NEUSTEIN LARYNGOSCOPE is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Neustein Laryngoscope Ref K901164
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neutech Corp. have in the registry?
The registry currently lists 1 device for Neutech Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neutech Corp.'s devices?
Among its 1 most recently registered device, Neutech Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Neutech Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neutech Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Neutech Corp. in the registry?
The most recently registered devices listed for Neutech Corp. include NEUSTEIN LARYNGOSCOPE.