Macdonald Medical Devices, Inc.
Country not established
- Devices
- 1
What Macdonald Medical Devices, Inc. makes
Macdonald Medical Devices, Inc. manufactures the ONAT ballooned nasogastric tube, a device designed for gastric decompression and feeding in clinical settings. The tube features a balloon mechanism for secure placement within the stomach, intended for use in patients requiring enteral nutrition or drainage.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device. The ONAT ballooned nasogastric tube is listed in the FDA’s 510(k) database. Macdonald Medical Devices, Inc. is based in the United States.
Catalogue
Onat Ballooned Nasogastric Tube Ref K920262
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Macdonald Medical Devices, Inc. have in the registry?
The registry currently lists 1 device for Macdonald Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Macdonald Medical Devices, Inc.'s devices?
Among its 1 most recently registered device, Macdonald Medical Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Macdonald Medical Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Macdonald Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Macdonald Medical Devices, Inc. in the registry?
The most recently registered devices listed for Macdonald Medical Devices, Inc. include ONAT BALLOONED NASOGASTRIC TUBE.