# Temporary Percutaneous Transluminal Cerebral Artery Dilatation Device
> **Product code: QTK** · f · Unknown · —
## Classification
- **FDA Product Code:** QTK
- **Device class:** f
- **Regulation:** —
- **Review panel:** NE
- **Medical specialty:** Unknown
- **Submission type:** 6
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

Used to temporarily dilate and increase the diameter of cerebral arteries experiencing symptomatic vasospasm

## Market data
- **Cleared 510(k) submissions:** 0
- **Registered establishments:** 2
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=QTK)
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