The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Littmann Electronic Stethoscope, Model 4100.
| Device ID | K051790 |
| 510k Number | K051790 |
| Device Name: | 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 4100 |
| Classification | Stethoscope, Electronic |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Contact | Ginger Cantor |
| Correspondent | Ginger Cantor 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-07-01 |
| Decision Date | 2005-07-25 |
| Summary: | summary |