| K-number | K883718 |
| Device name | MERIT HI-FLEX(TM) |
| Applicant | Merit Medical Systems, Inc. |
| Product code | FPK |
| Device class | Class II |
| Decision date | Jan 30, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 880.5440 |
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