| K-number | K782114 |
| Device name | MONITOR, OXYCHEK OXYGEN |
| Applicant | Critikon Company, LLC |
| Product code | CCL |
| Device class | Class II |
| Decision date | Jan 18, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 868.1720 |
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