Adam Spence Corp. · Class II · Cleared Jul 15, 1999
| K-number | K983940 |
| Device name | EZ-INTRO PERCUTANEOUS CATHETER SHEATH, EZ-INTRO VESSEL DILATOR |
| Applicant | Adam Spence Corp. |
| Product code | DYB |
| Device class | Class II |
| Decision date | Jul 15, 1999 |
| 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