Electro-Catheter Corp.
United StatesFDA applicant, unverified
- Devices
- 35
What Electro-Catheter Corp. makes
Electro-Catheter Corp. makes cardiac and vascular catheters, including pacing catheters such as the MULTIPACE and ELECATH(R) TRANSESOPHAGEAL PACING CATHETER, heparin-coated catheters, infant arterial and venous cannulas, semi-floating pacing kits, tip deflectors, dual-pressure bipolar pacing wedges, fluid-drain assemblies, and catheter introducer kits. The company also produces biliary and portal vein drainage assemblies and the BAIM Coronary Sinus Flow Analyzer.
The devices are classified as Class I, Class II, and Class III and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 35 devicesFrequently asked questions
How many devices does Electro-Catheter Corp. have in the registry?
The registry currently lists 35 devices for Electro-Catheter Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electro-Catheter Corp.'s devices?
Among its 35 most recently registered devices, Electro-Catheter Corp. has devices listed in FDA 510(k) (35 devices).
What risk classes do Electro-Catheter Corp.'s devices fall under?
Among its 35 most recently registered devices, the classes recorded for Electro-Catheter Corp.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Electro-Catheter Corp. in the registry?
The most recently registered devices listed for Electro-Catheter Corp. include MULTIPACE, ELECATH(R) TRANSESOPHAGEAL PACING CATHETER, ELECATH PORTAL VEIN/BILIARY DRAIN ASSM and ELECATH HEPARIN-COATED CATHETERS.