| K-number | K843559 |
| Device name | KLEENIT BY QMED |
| Applicant | Qmed, Inc. |
| Product code | — |
| Device class | Class unclassified |
| Decision date | Oct 24, 1984 |
| Decision | Substantially Equivalent |
| Regulation | — |
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