Kimberly-Clark Corp. · Class II · Cleared Apr 22, 2008
| K-number | K080821 |
| Device name | MICROCUFF PEDIATRIC ENDOTRACHEAL TUBE |
| Applicant | Kimberly-Clark Corp. |
| Product code | BTR |
| Device class | Class II |
| Decision date | Apr 22, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 868.5730 |
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