Synectics AB
SwedenFDA 510(k) applicant, unverified
- Devices
- 1
What Synectics AB makes
Synectics AB makes the Synectics PH & Pressure Esophageal Monitor, a device used to measure pH and pressure in the esophagus.
The device is classified as Class I and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Synectics Ph & Pressure Esophageal Monit Ref K842690
510(k) 510(k)
Frequently asked questions
How many devices does Synectics AB have in the registry?
The registry currently lists 1 device for Synectics AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synectics AB's devices?
Among its 1 most recently registered device, Synectics AB has devices listed in FDA 510(k) (1 device).
What risk classes do Synectics AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Synectics AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Synectics AB in the registry?
The most recently registered devices listed for Synectics AB include SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT.