The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Littmann Telesteth Online Ausculation System.
| Device ID | K120704 |
| 510k Number | K120704 |
| Device Name: | 3M LITTMANN TELESTETH ONLINE AUSCULATION SYSTEM |
| Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Contact | Jon Platt |
| Correspondent | Jon Platt 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Product Code | DRG |
| CFR Regulation Number | 870.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-08 |
| Decision Date | 2012-05-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00707387766597 | K120704 | 000 |