Healthwatch, Ltd.
Country not established FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Healthwatch, Ltd. makes
Healthwatch, Ltd. manufactures the Master Caution Device (MCD), a Class II medical device designed to alert operators to system malfunctions or safety alerts in medical equipment.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process, with the MCD classified as a Class II device. The company is based in the United States.
Catalogue
Cambridge Pc/Gxt Stress Test System Ref K921331
Regimes: 510(k) Registry: 510(k)Pacer Model 100 Infusion Controller Ref K963136
Regimes: 510(k) Registry: 510(k)Master Caution Device MCD Ref K142476
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Healthwatch Kfar Saba Central · IL FEI 3010363430
Frequently asked questions
How many devices does Healthwatch, Ltd. have in the registry?
The registry currently lists 3 devices for Healthwatch, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Healthwatch, Ltd.'s devices?
Among its 3 most recently registered devices, Healthwatch, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Healthwatch, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Healthwatch, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Healthwatch, Ltd. in the registry?
The most recently registered devices listed for Healthwatch, Ltd. include CAMBRIDGE PC/GXT STRESS TEST SYSTEM, PACER MODEL 100 INFUSION CONTROLLER and Master Caution Device MCD.
Which FDA establishments are linked to Healthwatch, Ltd.?
1 FDA establishment is linked to Healthwatch, Ltd. in the registry; they are listed on the company page.