Reimers Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Reimers Systems, Inc. makes
Reimers Systems, Inc. makes hyperbaric facilities and related equipment, including the T Class Hyperbaric Facility, LifeForce Clinical Hyperbaric Facility, RSI 4200, ODS1 - Hood Driver, and GSP1 - Gas Selection Panel.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Rsi 4200 Ref K102831
Regimes: 510(k) Registry: 510(k)ODS1 - Hood Driver Ref K962871
Regimes: 510(k) Registry: 510(k)T Class Hyperbaric Facilities Ref K954387
Regimes: 510(k) Registry: 510(k)GSP1 - Gas Selection Panel Ref K962869
Regimes: 510(k) Registry: 510(k)Lifeforce Clinical Hyperbaric Facility Ref K951125
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reimers Systems, Inc. have in the registry?
The registry currently lists 5 devices for Reimers Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reimers Systems, Inc.'s devices?
Among its 5 most recently registered devices, Reimers Systems, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Reimers Systems, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Reimers Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reimers Systems, Inc. in the registry?
The most recently registered devices listed for Reimers Systems, Inc. include RSI 4200, ODS1 - HOOD DRIVER, T CLASS HYPERBARIC FACILITIES and GSP1 - GAS SELECTION PANEL.