Shiley, Inc. · Class II · Cleared Mar 23, 1987
| K-number | K870826 |
| Device name | ADDITIONAL LETTER DESIGNATION FOR AORTIC ARCH CAN. |
| Applicant | Shiley, Inc. |
| Product code | DQR |
| Device class | Class II |
| Decision date | Mar 23, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 870.1300 |
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