Extravakit, Inc.
Country not established
- Devices
- 1
What Extravakit, Inc. makes
Extravakit, Inc. manufactures the Modified Extravakit, a medical device designed for vascular access and fluid management in clinical settings. This product is intended for use in procedures requiring controlled infusion or withdrawal of fluids, such as hemodialysis or blood sampling.
The Modified Extravakit falls under FDA Class II regulation and is listed via the 510(k) clearance pathway. The company is based in the United States, where its devices are registered and subject to compliance with U.S. medical device regulations.
Catalogue
Modified Extravakit Ref K882025
510(k) 510(k)
Frequently asked questions
How many devices does Extravakit, Inc. have in the registry?
The registry currently lists 1 device for Extravakit, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Extravakit, Inc.'s devices?
Among its 1 most recently registered device, Extravakit, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Extravakit, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Extravakit, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Extravakit, Inc. in the registry?
The most recently registered devices listed for Extravakit, Inc. include MODIFIED EXTRAVAKIT.