Drip Alert, Inc.
Country not established
- Devices
- 1
What Drip Alert, Inc. makes
Drip Alert, Inc. manufactures medical devices designed to monitor and alert healthcare providers to intravenous (IV) fluid administration issues, such as infusion rate abnormalities or disconnections. The primary product, Drip Alert, integrates with IV infusion pumps to detect irregularities in fluid delivery, helping prevent complications like under- or over-infusion.
The company’s portfolio is regulated under Class II devices in the United States, with products authorised through the FDA’s 510(k) clearance process. The devices are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Drip Alert Ref K030136
510(k) 510(k)
Frequently asked questions
How many devices does Drip Alert, Inc. have in the registry?
The registry currently lists 1 device for Drip Alert, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Drip Alert, Inc.'s devices?
Among its 1 most recently registered device, Drip Alert, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Drip Alert, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Drip Alert, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Drip Alert, Inc. in the registry?
The most recently registered devices listed for Drip Alert, Inc. include DRIP ALERT.