Pearlduck, Inc.
Country not established
- Devices
- 1
What Pearlduck, Inc. makes
Pearlduck, Inc. manufactures the Blood Pressure Kit, Well-BE 669, a device designed for measuring and monitoring blood pressure in clinical or home settings.
The company’s portfolio is regulated under FDA’s Class II designation and includes devices listed via the 510(k) pathway. Pearlduck, Inc. is based in the United States.
Catalogue
Blood Pressure Kit, Well-Be 669 Ref K761274
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pearlduck, Inc. have in the registry?
The registry currently lists 1 device for Pearlduck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pearlduck, Inc.'s devices?
Among its 1 most recently registered device, Pearlduck, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pearlduck, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pearlduck, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pearlduck, Inc. in the registry?
The most recently registered devices listed for Pearlduck, Inc. include BLOOD PRESSURE KIT, WELL-BE 669.