Sentron, Inc.
Country not established
- Devices
- 1
What Sentron, Inc. makes
Sentron, Inc. manufactures modifications to a series of cardiac catheters, which are used in interventional cardiology procedures for diagnostic and therapeutic applications, including coronary angiography and percutaneous coronary interventions.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Modifications To Series Of Cardiac Catheters Ref K913042
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sentron, Inc. have in the registry?
The registry currently lists 1 device for Sentron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sentron, Inc.'s devices?
Among its 1 most recently registered device, Sentron, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sentron, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sentron, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sentron, Inc. in the registry?
The most recently registered devices listed for Sentron, Inc. include MODIFICATIONS TO SERIES OF CARDIAC CATHETERS.