Penumbra, Inc. · Class II · Cleared Oct 4, 2022
| K-number | K220683 |
| Device name | INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4) |
| Applicant | Penumbra, Inc. |
| Product code | QEW |
| Device class | Class II |
| Decision date | Oct 4, 2022 |
| Decision | Unknown |
| Regulation | 870.5150 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov