Medtronic Inc. Cardiac Rhythm Management
United StatesFDA applicant, unverified
- Devices
- 2
What Medtronic Inc. Cardiac Rhythm Management makes
The company produces deflectable catheter systems for precise cardiac procedures, including models designed for enhanced navigation and positioning within the heart. It also manufactures hybrid guide wires, such as specific models for improved steerability and stability during interventions.
These devices are classified as Class II under regulatory frameworks and are listed via FDA 510(k) clearance. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Inc. Cardiac Rhythm Management have in the registry?
The registry currently lists 2 devices for Medtronic Inc. Cardiac Rhythm Management. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Inc. Cardiac Rhythm Management's devices?
Among its 2 most recently registered devices, Medtronic Inc. Cardiac Rhythm Management has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtronic Inc. Cardiac Rhythm Management's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtronic Inc. Cardiac Rhythm Management's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Inc. Cardiac Rhythm Management in the registry?
The most recently registered devices listed for Medtronic Inc. Cardiac Rhythm Management include MEDTRONIC SELECTSITE DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59 AND C304-L69 and ATTAIN HYBRID GUIDE WIRES, MODEL GWR419378, GWR419388, GWR419478, GWR419488.