Product code
PRC: Drug-coated peripheral transluminal angioplasty catheter
FDA product code · Class III · Cardiovascular
Key facts
| Product code | PRC |
|---|---|
| Device | Drug-coated peripheral transluminal angioplasty catheter |
| Device class | Class III |
| Review panel | Cardiovascular |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Balloon dilatation of native and/or synthetic arteriovenous dialysis fistulae to establish or maintain patency |
At a glance
- None 510(k) clearances
- None De Novo grants
- 1–9 PMA approvals
- None HDE approvals
- 100–999 UDI devices (GUDID)
- 100–999 MAUDE adverse event reports
- 1–9 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database