The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Littmann Electronic Stethoscope, Model 3000.
| Device ID | K041934 |
| 510k Number | K041934 |
| Device Name: | 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000 |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-07-19 |
| Decision Date | 2004-10-15 |
| Summary: | summary |