Medtronic-Synectics
SwedenFDA applicant, unverified
- Devices
- 1
What Medtronic-Synectics makes
Medtronic-Synectics makes an anorectal manometry analysis module, a device used to measure and analyze pressure and muscle activity in the rectum and anal canal for diagnostic purposes.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Anorectal Manometry Analysis Module Ref K972439
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic-Synectics have in the registry?
The registry currently lists 1 device for Medtronic-Synectics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic-Synectics's devices?
Among its 1 most recently registered device, Medtronic-Synectics has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic-Synectics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic-Synectics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic-Synectics in the registry?
The most recently registered devices listed for Medtronic-Synectics include ANORECTAL MANOMETRY ANALYSIS MODULE.