Omnicon Medical Corp. · Class I · Cleared Jan 12, 1977
| K-number | K770001 |
| Device name | AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S |
| Applicant | Omnicon Medical Corp. |
| Product code | CAE |
| Device class | Class I |
| Decision date | Jan 12, 1977 |
| Decision | Substantially Equivalent |
| Regulation | 868.5110 |
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