| K-number | K171245 |
| Device name | Presygen/si-1 |
| Applicant | Christie Medical Holdings, Inc. |
| Product code | MUD |
| Device class | Class II |
| Decision date | Aug 9, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 870.2700 |
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