Quinton Electrophysiology Corp.
Country not established
- Devices
- 3
What Quinton Electrophysiology Corp. makes
Quinton Electrophysiology Corp. manufactures electrophysiology (EP) amplifiers, including the Model #901, and systems like the EPXPRESS (Timberwolf Revision) for cardiac electrophysiology procedures. They also produce EPLAB, an electrocardiographic monitoring device designed for real-time cardiac signal recording.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Ep Amp, Model #901 Ref K925346
510(k) 510(k)Epxpress System (Timberwolf Revision) /000391 Ref K971570
510(k) 510(k)Eplab (Electrocardiographic Monitor) Ref K893836
510(k) 510(k)
Frequently asked questions
How many devices does Quinton Electrophysiology Corp. have in the registry?
The registry currently lists 3 devices for Quinton Electrophysiology Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quinton Electrophysiology Corp.'s devices?
Among its 3 most recently registered devices, Quinton Electrophysiology Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Quinton Electrophysiology Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Quinton Electrophysiology Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quinton Electrophysiology Corp. in the registry?
The most recently registered devices listed for Quinton Electrophysiology Corp. include EP AMP, MODEL #901, EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391 and EPLAB (ELECTROCARDIOGRAPHIC MONITOR).