James J. Lally
Country not established
- Devices
- 1
What James J. Lally makes
James J. Lally manufactures pulse-aid devices designed for therapeutic or diagnostic applications, including those used in vascular or neurological interventions.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. Its devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Pulse-Aid Device Ref K843977
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does James J. Lally have in the registry?
The registry currently lists 1 device for James J. Lally. Devices recorded under merged duplicate company entries are counted once.
Which registries list James J. Lally's devices?
Among its 1 most recently registered device, James J. Lally has devices listed in FDA 510(k) (1 device).
What risk classes do James J. Lally's devices fall under?
Among its 1 most recently registered device, the classes recorded for James J. Lally's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from James J. Lally in the registry?
The most recently registered devices listed for James J. Lally include PULSE-AID DEVICE.