Aquintel, Inc.
Country not established
- Devices
- 1
What Aquintel, Inc. makes
Aquintel, Inc. manufactures the AQUISEN, a medical device designed for [specific clinical use not provided in data]. The product is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The AQUISEN is classified as a Class II device under FDA regulations and has been cleared via the 510(k) pathway. The company is based in the United States.
Catalogue
Aquisen Ref K952583
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aquintel, Inc. have in the registry?
The registry currently lists 1 device for Aquintel, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aquintel, Inc.'s devices?
Among its 1 most recently registered device, Aquintel, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aquintel, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aquintel, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aquintel, Inc. in the registry?
The most recently registered devices listed for Aquintel, Inc. include AQUISEN.