Sauquoit Industries, Inc.
Country not established
- Devices
- 1
What Sauquoit Industries, Inc. makes
Sauquoit Industries, Inc. manufactures disposable DTL (Direct Tissue Lead) electrodes, which are used for electrocardiogram (ECG) monitoring to attach to a patient’s skin and transmit electrical signals from the heart.
The company’s DTL electrodes are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is registered in the U.S., where the manufacturer is based.
Catalogue
Dtl Electrode Ref K844409
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sauquoit Industries, Inc. have in the registry?
The registry currently lists 1 device for Sauquoit Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sauquoit Industries, Inc.'s devices?
Among its 1 most recently registered device, Sauquoit Industries, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sauquoit Industries, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sauquoit Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sauquoit Industries, Inc. in the registry?
The most recently registered devices listed for Sauquoit Industries, Inc. include DTL ELECTRODE.