Kontron Instruments, Inc. · Class II · Cleared Sep 27, 1993
| K-number | K925248 |
| Device name | MODIFICATION OF INTRA-AORTIC BALLOON CATHETERS |
| Applicant | Kontron Instruments, Inc. |
| Product code | DSP |
| Device class | Class II |
| Decision date | Sep 27, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 870.3535 |
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