Ventrex Laboratories, Inc. · Class II · Cleared Apr 23, 1979
| K-number | K790447 |
| Device name | VENTRE/SEP FERRITIN RIA |
| Applicant | Ventrex Laboratories, Inc. |
| Product code | DBF |
| Device class | Class II |
| Decision date | Apr 23, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 866.5340 |
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