The following data is part of a premarket notification filed by 3m Company with the FDA for Modification To: 3m Littmann Electronic Stethoscope, Model 3000.
| Device ID | K050159 |
| 510k Number | K050159 |
| Device Name: | MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000 |
| Classification | Stethoscope, Electronic |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Contact | Ginger Cantor |
| Correspondent | Ginger Cantor 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 | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-01-25 |
| Decision Date | 2005-02-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50707387765557 | K050159 | 000 |
| 50707387765540 | K050159 | 000 |
| 50707387765533 | K050159 | 000 |
| 50707387765472 | K050159 | 000 |
| 50707387765465 | K050159 | 000 |
| 50707387765458 | K050159 | 000 |