Davis & Geck, Inc. · Class II · Cleared Mar 20, 1998
| K-number | K980062 |
| Device name | MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE |
| Applicant | Davis & Geck, Inc. |
| Product code | FMI |
| Device class | Class II |
| Decision date | Mar 20, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 880.5570 |
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