Tandem Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tandem Medical, Inc. makes
Tandem Medical, Inc. manufactures the AUTODOSE INFUSION SYSTEM, including models AD4120, BE4210, S12050, 100, 200, FF0005, and 10.
The company's devices are Class II and listed in the FDA 510(k) registry. Tandem Medical is based in the US.
Catalogue
Autodose Infusion System Ref K990889
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tandem Medical, Inc. have in the registry?
The registry currently lists 2 devices for Tandem Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tandem Medical, Inc.'s devices?
Among its 2 most recently registered devices, Tandem Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tandem Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tandem Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tandem Medical, Inc. in the registry?
The most recently registered devices listed for Tandem Medical, Inc. include AUTODOSE INFUSION SYSTEM and AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050, 100, 200, FF0005, 10.