Nautilus Environmedical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Nautilus Environmedical Systems, Inc. makes
Nautilus Environmedical Systems, Inc. manufactures monoplace hyperbaric units designed for medical oxygen therapy under pressure, as well as ventilator systems integrated with hyperbaric chambers for patient care in controlled environments.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States.
Catalogue
Nautilus Monoplace Hyperbaric Unit Ref K832127
Regimes: 510(k) Registry: 510(k)Sechrist Ventilator/Nautilus Chamber Combination Ref K850563
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nautilus Environmedical Systems, Inc. have in the registry?
The registry currently lists 2 devices for Nautilus Environmedical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nautilus Environmedical Systems, Inc.'s devices?
Among its 2 most recently registered devices, Nautilus Environmedical Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nautilus Environmedical Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nautilus Environmedical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nautilus Environmedical Systems, Inc. in the registry?
The most recently registered devices listed for Nautilus Environmedical Systems, Inc. include NAUTILUS MONOPLACE HYPERBARIC UNIT and SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION.