Kontron Instruments, Inc. · Class II · Cleared Mar 8, 1993
| K-number | K923603 |
| Device name | INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION |
| Applicant | Kontron Instruments, Inc. |
| Product code | DYB |
| Device class | Class II |
| Decision date | Mar 8, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 870.1340 |
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