Mechidyne Systems, Inc.
Country not established
- Devices
- 1
What Mechidyne Systems, Inc. makes
Mechidyne Systems, Inc. manufactures the MSI I2010, a dual-place hyperbaric chamber designed for medical oxygen therapy under pressure.
The company’s products are regulated as Class II devices in the US and are listed under FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Msi I2010 Dual Place Hyperbaric Chamber Ref K022214
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mechidyne Systems, Inc. have in the registry?
The registry currently lists 1 device for Mechidyne Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mechidyne Systems, Inc.'s devices?
Among its 1 most recently registered device, Mechidyne Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mechidyne Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mechidyne Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mechidyne Systems, Inc. in the registry?
The most recently registered devices listed for Mechidyne Systems, Inc. include MSI I2010 DUAL PLACE HYPERBARIC CHAMBER.