Holden Walker Corp.
Country not established
- Devices
- 1
What Holden Walker Corp. makes
Holden Walker Corp. manufactures the Holden-Walker Humidifier-Nebulizer Kit, a device designed for delivering aerosolized medication or hydration to patients via inhalation.
The company’s portfolio is regulated under Class II devices in the US and includes products listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Holden-Walker Humidifier-Nebulizer Kit Ref K963917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Holden Walker Corp. have in the registry?
The registry currently lists 1 device for Holden Walker Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Holden Walker Corp.'s devices?
Among its 1 most recently registered device, Holden Walker Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Holden Walker Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Holden Walker Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Holden Walker Corp. in the registry?
The most recently registered devices listed for Holden Walker Corp. include HOLDEN-WALKER HUMIDIFIER-NEBULIZER KIT.