The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Littmann.
| Device ID | K003723 |
| 510k Number | K003723 |
| Device Name: | 3M LITTMANN |
| Classification | Stethoscope, Electronic |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Contact | Linda Johnsen |
| Correspondent | Linda Johnsen 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-04 |
| Decision Date | 2001-03-27 |