Medcon, Ltd.
Country not established
- Devices
- 6
What Medcon, Ltd. makes
Medcon, Ltd. manufactures medical imaging and telecardiology systems, including a DICOM-compatible viewer for diagnostic images and an ECG management platform for cardiology workflows. Their portfolio also includes a telecardiology system for remote cardiac monitoring and a portable ECG device designed for clinical use.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. These products are listed in the FDA’s regulatory database and are based in the United States.
Catalogue
Medcuff Ref K942488
Regimes: 510(k) Registry: 510(k)Windsurfer Ref K050561
Regimes: 510(k) Registry: 510(k)Cleancuff(Tm) Ref K931087
Regimes: 510(k) Registry: 510(k)The Midview-Medcon's Dicom Viewer Ref K971181
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
The Tcs-Medcon's Telecardiology System Ref K974679
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medcon, Ltd. have in the registry?
The registry currently lists 6 devices for Medcon, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcon, Ltd.'s devices?
Among its 6 most recently registered devices, Medcon, Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Medcon, Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Medcon, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medcon, Ltd. in the registry?
The most recently registered devices listed for Medcon, Ltd. include MEDCUFF, WINDSURFER, CLEANCUFF(TM) and THE MIDVIEW-MEDCON'S DICOM VIEWER.