Paraworks Enterprise, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Paraworks Enterprise, Ltd. makes
Paraworks Enterprise, Ltd. manufactures the A PHARNESS, a Class I medical device designed for patient attachment and mobility support in clinical settings.
The device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
A P Harness Ref K981860
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paraworks Enterprise, Ltd. have in the registry?
The registry currently lists 1 device for Paraworks Enterprise, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paraworks Enterprise, Ltd.'s devices?
Among its 1 most recently registered device, Paraworks Enterprise, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Paraworks Enterprise, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Paraworks Enterprise, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Paraworks Enterprise, Ltd. in the registry?
The most recently registered devices listed for Paraworks Enterprise, Ltd. include A P HARNESS.