FDA product code QCT: Scaffold, Dissection Repair
QCT is the FDA product code for scaffold, dissection repair. It is a Class III device, reviewed by the Cardiovascular panel. Devices under QCT reach the market by PMA; FDA lists no cleared 510(k)s for it. 2 PMA applications cite this product code. FDA has posted 1 recall for QCT devices, 1 initiated in the last five years.
Definition
For the repair of dissections following percutaneous transluminal angioplasty in the lower extremity arteries
Classification
| Field | Value |
|---|---|
| Device name | Scaffold, Dissection Repair |
| Device class | Class III |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | PMA |
| Implant | Yes |
| Life-sustaining or supporting | Yes |
Recalls for QCT devices
1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2025-01-10.
| Year | Recalls |
|---|---|
| 2025 | 1 |
Frequently asked questions
What is FDA product code QCT?
QCT is the FDA product code for scaffold, dissection repair. It is a Class III device, reviewed by the Cardiovascular panel.
What device class is QCT?
Class III. Typical premarket route: PMA.
Have QCT devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2025-01-10.
Next steps
- Run an FDA pathway report with predicate devices for product code QCT
- Run a recall and safety report across every QCT manufacturer
- Watch product code QCT for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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