Avi, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 13
What Avi, Inc. makes
Avi, Inc. manufactures a range of programmable infusion pumps designed for controlled delivery of fluids, including the AVI GUARDIAN MICRO 410, MODEL 200A, and ENTRUST™ Model 800. These devices support volumetric control systems for precise medication or fluid administration, such as the GUARDIAN 110 and various MODEL 200/400 series pumps. Additional models like the INFUSION PUMP MODEL 470 and 270 cater to specialized infusion needs in clinical settings.
The company’s infusion pumps are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. These devices are listed in the FDA’s 510(k) database, reflecting their regulatory authorization for commercial distribution in the United States.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Avi, Inc. have in the registry?
The registry currently lists 13 devices for Avi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avi, Inc.'s devices?
Among its 13 most recently registered devices, Avi, Inc. has devices listed in FDA 510(k) (13 devices).
What risk classes do Avi, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Avi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avi, Inc. in the registry?
The most recently registered devices listed for Avi, Inc. include AVI GUARDIAN MICRO 410 INFUSION PUMP, MODEL 200A INFUSION PUMP, ENTRUST(TM) MODEL 800 and GUARDIAN, VOLUMETRIC CONTROL DELIVERY.