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Cryogenic Assoc.

Country not established

Devices
6

What Cryogenic Assoc. makes

Cryogenic Assoc. manufactures respiratory equipment including portable gaseous oxygen containers, oxygen concentrators, and liquid oxygen systems such as the Liberator/Stroller II and Stroller Sprint. These products are designed for the storage and delivery of supplemental oxygen to patients.

The company is based in the United States and maintains a portfolio of Class I and Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

  • Portable Gaseous Oxgyen Container Ref K852663

    Class I
    Active 510(k) 510(k) I
  • Roommate-Oxygen Concentrator Ref K801104

    Class II
    Active 510(k) 510(k) II
  • Oxytrol Ref K883590

    Class II
    Active 510(k) 510(k) II
  • Liberator/Stroller Ii System Ref K800742

    Class II
    Active 510(k) 510(k) II
  • Stroller Sprint Ref K841808

    Class II
    Active 510(k) 510(k) II
  • Roomate Ii Ref K822789

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Cryogenic Assoc. have in the registry?

The registry currently lists 6 devices for Cryogenic Assoc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cryogenic Assoc.'s devices?

Among its 6 most recently registered devices, Cryogenic Assoc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Cryogenic Assoc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Cryogenic Assoc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cryogenic Assoc. in the registry?

The most recently registered devices listed for Cryogenic Assoc. include PORTABLE GASEOUS OXGYEN CONTAINER, ROOMMATE-OXYGEN CONCENTRATOR, OXYTROL and LIBERATOR/STROLLER II SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.