| K-number | K170820 |
| Device name | Capnograph and Oximeter |
| Applicant | Cmi Health, Inc. |
| Product code | CCK |
| Device class | Class II |
| Decision date | Jul 18, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 868.1400 |
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