Bard Interventional Products Div.
Country not established
- Devices
- 2
What Bard Interventional Products Div. makes
The company manufactures papillotomes, including pre-curved models (PROFORMA and APOLLO series) and a high-flow variant, designed for biliary or pancreatic duct interventions.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Bard Proforma And Apollo Pre-Curved Papillotomes Ref K982557
Regimes: 510(k) Registry: 510(k)Bard High Flow Papillotome Ref K963484
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bard Interventional Products Div. have in the registry?
The registry currently lists 2 devices for Bard Interventional Products Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bard Interventional Products Div.'s devices?
Among its 2 most recently registered devices, Bard Interventional Products Div. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bard Interventional Products Div.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bard Interventional Products Div.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bard Interventional Products Div. in the registry?
The most recently registered devices listed for Bard Interventional Products Div. include BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES and BARD HIGH FLOW PAPILLOTOME.