Lineberger External Catheter Co. · Class II · Cleared Jun 20, 1980
| K-number | K800890 |
| Device name | LINEBERGER EXTERNAL MALE CATHETER |
| Applicant | Lineberger External Catheter Co. |
| Product code | KNX |
| Device class | Class II |
| Decision date | Jun 20, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 876.5250 |
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