Wayne V. Kirkman
Country not established
- Devices
- 1
What Wayne V. Kirkman makes
Wayne V. Kirkman manufactures paraplegic beds designed for patients with spinal cord injuries or mobility impairments. These beds provide adjustable positioning and support to enhance comfort and reduce pressure injuries for long-term use.
The paraplegic bed falls under Class II regulatory classification in the US and is listed via FDA 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Bed, Paraplegic Ref K790049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wayne V. Kirkman have in the registry?
The registry currently lists 1 device for Wayne V. Kirkman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wayne V. Kirkman's devices?
Among its 1 most recently registered device, Wayne V. Kirkman has devices listed in FDA 510(k) (1 device).
What risk classes do Wayne V. Kirkman's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wayne V. Kirkman's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wayne V. Kirkman in the registry?
The most recently registered devices listed for Wayne V. Kirkman include BED, PARAPLEGIC.