Deknatel, Inc. · Class II · Cleared Apr 4, 1989
| K-number | K890431 |
| Device name | PLEUR-EVAC(R) A-8000--ADULT/PEDIATRIC CHEST DRAIN |
| Applicant | Deknatel, Inc. |
| Product code | GCX |
| Device class | Class II |
| Decision date | Apr 4, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 880.6740 |
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