Smi Patientcare, Inc.
Country not established
- Devices
- 1
What Smi Patientcare, Inc. makes
Smi Patientcare, Inc. manufactures the SMI 3000 AIRBED, a medical air mattress designed for patient support and pressure redistribution to prevent pressure ulcers.
The SMI 3000 AIRBED is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Smi 3000 Airbed Ref K883192
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smi Patientcare, Inc. have in the registry?
The registry currently lists 1 device for Smi Patientcare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smi Patientcare, Inc.'s devices?
Among its 1 most recently registered device, Smi Patientcare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Smi Patientcare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Smi Patientcare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smi Patientcare, Inc. in the registry?
The most recently registered devices listed for Smi Patientcare, Inc. include SMI 3000 AIRBED.