| K-number | K953593 |
| Device name | RUSCH TRACHEAL BRONCHIAL Y STENT |
| Applicant | Rusch, Inc. |
| Product code | NYT |
| Device class | Class II |
| Decision date | Oct 13, 1995 |
| Decision | Substantially Equivalent - Subject to Tracking Reg. |
| Regulation | 878.3720 |
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