Yeescope Pty., Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
What Yeescope Pty., Ltd. makes
Yeescope manufactures laryngoscopes, which are medical devices used for visualizing the larynx during procedures such as intubation or airway assessment.
The company’s laryngoscopes are classified as Class I devices under FDA regulations and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Yeescope Laryngoscopes Ref K140951
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Yeescope Pty., Ltd. have in the registry?
The registry currently lists 1 device for Yeescope Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yeescope Pty., Ltd.'s devices?
Among its 1 most recently registered device, Yeescope Pty., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Yeescope Pty., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Yeescope Pty., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Yeescope Pty., Ltd. in the registry?
The most recently registered devices listed for Yeescope Pty., Ltd. include YEESCOPE LARYNGOSCOPES.