Atlantean Corporation
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Atlantean Corporation makes
Atlantean Corporation manufactures the Atlantean Trigger Nebulizer, a handheld device designed for delivering inhaled medication in aerosol form to patients.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. Atlantean Corporation is based in the United States.
Catalogue
Model SB100II Finger Pulse Oximeter Ref K101568
510(k) 510(k)Atlantean Trigger Nebulizer Ref K102719
510(k) 510(k)
Frequently asked questions
How many devices does Atlantean Corporation have in the registry?
The registry currently lists 2 devices for Atlantean Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Atlantean Corporation's devices?
Among its 2 most recently registered devices, Atlantean Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Atlantean Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Atlantean Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Atlantean Corporation in the registry?
The most recently registered devices listed for Atlantean Corporation include MODEL SB100II FINGER PULSE OXIMETER and ATLANTEAN TRIGGER NEBULIZER.