Acu-Pak
Country not established
- Devices
- 1
What Acu-Pak makes
Acu-Pak manufactures sterile saline solution (0.9%) and sterile water for injection, supplied in catalog numbers 10290 and 10291 respectively.
These products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acu-Pak have in the registry?
The registry currently lists 1 device for Acu-Pak. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acu-Pak's devices?
Among its 1 most recently registered device, Acu-Pak has devices listed in FDA 510(k) (1 device).
What risk classes do Acu-Pak's devices fall under?
Among its 1 most recently registered device, the classes recorded for Acu-Pak's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acu-Pak in the registry?
The most recently registered devices listed for Acu-Pak include STERILE SALINE SOLUTION 0.9%- CATALOG NO, 10290, STERILE WATER- CATALOG NO. 10291.