Esb, Inc., Div. of Ray-O-Vac
Country not established
- Devices
- 1
What Esb, Inc., Div. of Ray-O-Vac makes
Esb, Inc. manufactures the ESB 2400 SEI, a self-expanding intraluminal stent designed for vascular applications, including peripheral and coronary arteries.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the U.S. under FDA regulations, with the company headquartered in the United States.
Catalogue
Esb 2400 Sei Ref K933146
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Esb, Inc., Div. of Ray-O-Vac have in the registry?
The registry currently lists 1 device for Esb, Inc., Div. of Ray-O-Vac. Devices recorded under merged duplicate company entries are counted once.
Which registries list Esb, Inc., Div. of Ray-O-Vac's devices?
Among its 1 most recently registered device, Esb, Inc., Div. of Ray-O-Vac has devices listed in FDA 510(k) (1 device).
What risk classes do Esb, Inc., Div. of Ray-O-Vac's devices fall under?
Among its 1 most recently registered device, the classes recorded for Esb, Inc., Div. of Ray-O-Vac's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Esb, Inc., Div. of Ray-O-Vac in the registry?
The most recently registered devices listed for Esb, Inc., Div. of Ray-O-Vac include ESB 2400 SEI.