Baxter Healthcare Corp · Class II · Cleared Oct 18, 1993
| K-number | K931464 |
| Device name | BAXTER CORONARY ANGIOSCOPE INFLATION DEVICE |
| Applicant | Baxter Healthcare Corp |
| Product code | LYK |
| Device class | Class II |
| Decision date | Oct 18, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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