| K-number | K003723 |
| Device name | 3M LITTMANN |
| Applicant | 3M Company |
| Product code | DQD |
| Device class | Class II |
| Decision date | Mar 27, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 870.1875 |
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