Applied Membrane Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Applied Membrane Technology, Inc. makes
Applied Membrane Technology, Inc. manufactures respiratory monitoring and oxygen delivery devices, including adult apnea monitors with interface units, a demand oxygen system (SAUER DOS2 Model 10), and a demand oxygen saver system (D02S). These products are designed for continuous patient monitoring and controlled oxygen administration in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
Adult Apnea Monitor (20), Monitor Interface (30) Ref K870835
Regimes: 510(k) Registry: 510(k)Demand Oxygen Sauer DOS2 Model 10 Ref K851235
Regimes: 510(k) Registry: 510(k)Demand Oxygen Saver System (D02S) Ref K861423
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Membrane Technology, Inc. have in the registry?
The registry currently lists 3 devices for Applied Membrane Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Membrane Technology, Inc.'s devices?
Among its 3 most recently registered devices, Applied Membrane Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Applied Membrane Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Applied Membrane Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Membrane Technology, Inc. in the registry?
The most recently registered devices listed for Applied Membrane Technology, Inc. include ADULT APNEA MONITOR (20), MONITOR INTERFACE (30), DEMAND OXYGEN SAUER DOS2 MODEL 10 and DEMAND OXYGEN SAVER SYSTEM (D02S).