Patrick J. O'Regan
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Patrick J. O'Regan makes
The company manufactures the O’Regan Ligator, a surgical device used for tissue approximation and ligation in minimally invasive procedures, particularly in laparoscopic surgery.
The O’Regan Ligator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
O'regan Ligator Ref K963166
510(k) 510(k)
Frequently asked questions
How many devices does Patrick J. O'Regan have in the registry?
The registry currently lists 1 device for Patrick J. O'Regan. Devices recorded under merged duplicate company entries are counted once.
Which registries list Patrick J. O'Regan's devices?
Among its 1 most recently registered device, Patrick J. O'Regan has devices listed in FDA 510(k) (1 device).
What risk classes do Patrick J. O'Regan's devices fall under?
Among its 1 most recently registered device, the classes recorded for Patrick J. O'Regan's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Patrick J. O'Regan in the registry?
The most recently registered devices listed for Patrick J. O'Regan include O'REGAN LIGATOR.