Cranco Co.
Country not established
- Devices
- 1
What Cranco Co. makes
Cranco Co. manufactures the VETA/Vented Esophageal Tube Airway, a device designed for airway management in emergency medical situations, including cardiopulmonary resuscitation (CPR).
The VETA/Vented Esophageal Tube Airway is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Veta/Vented Esophageal Tube Airway Ref K864200
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cranco Co. have in the registry?
The registry currently lists 1 device for Cranco Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cranco Co.'s devices?
Among its 1 most recently registered device, Cranco Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Cranco Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cranco Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cranco Co. in the registry?
The most recently registered devices listed for Cranco Co. include VETA/VENTED ESOPHAGEAL TUBE AIRWAY.