Amluck, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Amluck, Inc. makes
Amluck, Inc. manufactures automatic digital wrist blood pressure monitors, including models AK-3000 and AK-4000, designed for home or clinical use to measure systolic and diastolic blood pressure.
These devices are classified as Class II under FDA regulations and are listed via the 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 Amluck, Inc. have in the registry?
The registry currently lists 1 device for Amluck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amluck, Inc.'s devices?
Among its 1 most recently registered device, Amluck, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Amluck, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Amluck, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amluck, Inc. in the registry?
The most recently registered devices listed for Amluck, Inc. include AMLUCK AUTOMATIC DIGITAL WRIST, BLOOD PRESSURE MONITOR AK-3000/AK-4000.