The following data is part of a premarket notification filed by Minnesota Mining And Mfg. Co. with the FDA for 3m Littmann Electronic Stethoscope.
| Device ID | K961848 |
| 510k Number | K961848 |
| Device Name: | 3M LITTMANN ELECTRONIC STETHOSCOPE |
| Classification | Stethoscope, Electronic |
| Applicant | MINNESOTA MINING AND MFG. CO. 3M CENTER, BUILDING 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 -3275 |
| Contact | Linda Jonsen |
| Correspondent | Linda Jonsen MINNESOTA MINING AND MFG. CO. 3M CENTER, BUILDING 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 -3275 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-13 |
| Decision Date | 1997-09-26 |
| Summary: | summary |