Cardinal Health 303, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cardinal Health 303, Inc. makes
Cardinal Health 303, Inc. manufactures infusion pumps, including the ALARIS PC Unit (models 8000 and 8015), the ALARIS System with MMS (model 8XXX), and the Signature Edition infusion systems (models 7X3X, 710X, and 720X). These devices are designed for intravenous fluid administration and medication delivery 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. The devices are listed in the FDA’s 510(k) database, reflecting their authorised status for commercial distribution in the United States.
Catalogue
Alaris Pc Unit, Models 8000 And 8015 Ref K091308
Regimes: 510(k) Registry: 510(k)Alaris System With Mms, Model 8XXX Ref K072105
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardinal Health 303, Inc. have in the registry?
The registry currently lists 4 devices for Cardinal Health 303, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardinal Health 303, Inc.'s devices?
Among its 4 most recently registered devices, Cardinal Health 303, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cardinal Health 303, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cardinal Health 303, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardinal Health 303, Inc. in the registry?
The most recently registered devices listed for Cardinal Health 303, Inc. include ALARIS PC UNIT, MODELS 8000 AND 8015, ALARIS SYSTEM WITH MMS, MODEL 8XXX, SIGNATURE EDITION GOLD INFUSION SYSTEM, MODEL 7X3X and SIGNATURE EDITION INFUSION SYSTEM, MODELS 710X, 720X.