Post Operative Pain Management
Country not established
- Devices
- 1
What Post Operative Pain Management makes
The company produces the P.O.P. PAIN KIT, a post-operative pain management solution designed for patient use following surgical procedures.
This product is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
P.O.P. Pain Kit Ref K001342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Post Operative Pain Management have in the registry?
The registry currently lists 1 device for Post Operative Pain Management. Devices recorded under merged duplicate company entries are counted once.
Which registries list Post Operative Pain Management's devices?
Among its 1 most recently registered device, Post Operative Pain Management has devices listed in FDA 510(k) (1 device).
What risk classes do Post Operative Pain Management's devices fall under?
Among its 1 most recently registered device, the classes recorded for Post Operative Pain Management's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Post Operative Pain Management in the registry?
The most recently registered devices listed for Post Operative Pain Management include P.O.P. PAIN KIT.