Vitaphore Corp. · Class II · Cleared Mar 29, 1989
| K-number | K890435 |
| Device name | VITAACCESS CATHETER INTRODUCER KIT |
| Applicant | Vitaphore Corp. |
| Product code | FOZ |
| Device class | Class II |
| Decision date | Mar 29, 1989 |
| Decision | Substantially Equivalent — Same Device |
| Regulation | 880.5200 |
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