Datex-Engstrom, Inc.
Also registered as Datex Engstrom AB
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cs/3(Tm) Monitors* Ref K974792
Regimes: 510(k) Registry: 510(k)Trip Tonometry Catheter, 18F Ref K980384
Regimes: 510(k) Registry: 510(k)Cs/3 Arrhythmia Workstation Ref K974747
Regimes: 510(k) Registry: 510(k)Engstrom Hmef 1000 Ref K964204
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Datex-Engstrom Network Ref K974101
Regimes: 510(k) Registry: 510(k)Trip Tonometry Catheter, 16F Ref K983366
Regimes: 510(k) Registry: 510(k)As/3 Anaesthesia Delivery Unit (As/3 Adu) Ref K973985
Regimes: 510(k) Registry: 510(k)Mri Compatible Monitor And Accessories Ref K980362
Regimes: 510(k) Registry: 510(k)Cs/3 Compact Airway Module, M-Covx Ref K982091
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Datex-Engstrom, Inc. have in the registry?
The registry currently lists 10 devices for Datex-Engstrom, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Datex-Engstrom, Inc.'s devices?
Among its 10 most recently registered devices, Datex-Engstrom, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Datex-Engstrom, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Datex-Engstrom, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Datex-Engstrom, Inc. in the registry?
The most recently registered devices listed for Datex-Engstrom, Inc. include CS/3(TM) MONITORS*, TRIP TONOMETRY CATHETER, 18F, CS/3 ARRHYTHMIA WORKSTATION and ENGSTROM HMEF 1000.