Crandall Medical Devices
Country not established
- Devices
- 1
What Crandall Medical Devices makes
Crandall Medical Devices makes medical devices such as percutaneous tracheostomy tube kits. These are specific types of medical products used for tracheostomy procedures.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Percutaneous Tracheostomy Tube Kit Ref K931611
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Crandall Medical Devices have in the registry?
The registry currently lists 1 device for Crandall Medical Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crandall Medical Devices's devices?
Among its 1 most recently registered device, Crandall Medical Devices has devices listed in FDA 510(k) (1 device).
What risk classes do Crandall Medical Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for Crandall Medical Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Crandall Medical Devices in the registry?
The most recently registered devices listed for Crandall Medical Devices include PERCUTANEOUS TRACHEOSTOMY TUBE KIT.