Cardio-Search, Ltd.
Country not established
- Devices
- 5
What Cardio-Search, Ltd. makes
Cardio-Search, Ltd. manufactures a flowmeter nipple adaptor, a component used in medical fluid management systems to connect tubing and ensure accurate flow measurement in respiratory or infusion therapies.
The company’s product is classified as Class I under FDA regulations and is listed in the FDA’s 510(k) clearance database. The manufacturer is based in the United States.
Catalogue
Eyrthrocath Double-Lumen Central Venous Ref K842133
Regimes: 510(k) Registry: 510(k)Venous Catheter Ref K832064
Regimes: 510(k) Registry: 510(k)Cardiosearch Right Atrial Cath- Ref K833873
Regimes: 510(k) Registry: 510(k)Erythrocath Umbilical Catheter Ref K841880
Regimes: 510(k) Registry: 510(k)Flowmeter Nipple Adaptor Ref K934945
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio-Search, Ltd. have in the registry?
The registry currently lists 5 devices for Cardio-Search, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio-Search, Ltd.'s devices?
Among its 5 most recently registered devices, Cardio-Search, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Cardio-Search, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cardio-Search, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio-Search, Ltd. in the registry?
The most recently registered devices listed for Cardio-Search, Ltd. include EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS, VENOUS CATHETER, CARDIOSEARCH RIGHT ATRIAL CATH- and ERYTHROCATH UMBILICAL CATHETER.