Vas-Cath, Inc. · Class II · Cleared Jul 1, 1993
| K-number | K914210 |
| Device name | VAS-CATH DUALATOR(TM) VESSEL DILATOR |
| Applicant | Vas-Cath, Inc. |
| Product code | FKA |
| Device class | Class II |
| Decision date | Jul 1, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 876.5540 |
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