| K-number | K220848 |
| Device name | Venue Fit |
| Applicant | GE Medical Systems |
| Product code | IYN |
| Device class | Class II |
| Decision date | Jun 27, 2022 |
| Decision | Substantially Equivalent |
| Regulation | 892.1550 |
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