Tursiop Technologies, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Tursiop Technologies, LLC makes
Tursiop Technologies, LLC manufactures MRI coils, including a general-purpose coil and a specialized carotid coil designed for use with 1.5T MRI systems. These devices are intended for imaging soft tissues and vascular structures in the neck region.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States.
Catalogue
TT1 General Purpose Coil Ref K083434
510(k) 510(k)Carotid Coil Ge 1.5T Ref K113280
510(k) 510(k)
Frequently asked questions
How many devices does Tursiop Technologies, LLC have in the registry?
The registry currently lists 2 devices for Tursiop Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tursiop Technologies, LLC's devices?
Among its 2 most recently registered devices, Tursiop Technologies, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Tursiop Technologies, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tursiop Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tursiop Technologies, LLC in the registry?
The most recently registered devices listed for Tursiop Technologies, LLC include TT1 GENERAL PURPOSE COIL and CAROTID COIL GE 1.5T.