Aicl-Pack, Inc.
Country not established
- Devices
- 1
What Aicl-Pack, Inc. makes
Aicl-Pack, Inc. manufactures in-home early pregnancy test devices designed for hospital lab and consumer use, providing rapid diagnostic results for detecting pregnancy at an early stage.
The company’s products fall under FDA Class II regulation and are listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Hospital Lab In-Home Early Preg Test Ref K832593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aicl-Pack, Inc. have in the registry?
The registry currently lists 1 device for Aicl-Pack, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aicl-Pack, Inc.'s devices?
Among its 1 most recently registered device, Aicl-Pack, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aicl-Pack, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aicl-Pack, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aicl-Pack, Inc. in the registry?
The most recently registered devices listed for Aicl-Pack, Inc. include HOSPITAL LAB IN-HOME EARLY PREG TEST.