QTK — Temporary Percutaneous Transluminal Cerebral Artery Dilatation Device Class f
FDA product code QTK covers "Temporary Percutaneous Transluminal Cerebral Artery Dilatation Device", a Class f medical device. Submissions are reviewed by the Unknown panel.
Classification Details
- Product Code
- QTK
- Device Class
- Class f
- Regulation Number
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Unknown
- Implant
- No
Definition
Used to temporarily dilate and increase the diameter of cerebral arteries experiencing symptomatic vasospasm