Hepacron, Inc.
Country not established
- Devices
- 1
What Hepacron, Inc. makes
Hepacron, Inc. manufactures the HEPACRON PUREAIR-ZONE SYSTEM, a device designed for air purification in controlled environments, likely targeting healthcare or laboratory settings to reduce airborne contaminants.
The company’s portfolio is regulated under FDA Class II devices, with the HEPACRON PUREAIR-ZONE SYSTEM authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Hepacron Pureair-Zone System Ref K862432
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hepacron, Inc. have in the registry?
The registry currently lists 1 device for Hepacron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hepacron, Inc.'s devices?
Among its 1 most recently registered device, Hepacron, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hepacron, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hepacron, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hepacron, Inc. in the registry?
The most recently registered devices listed for Hepacron, Inc. include HEPACRON PUREAIR-ZONE SYSTEM.