The following data is part of a premarket notification filed by Rsp, Inc. with the FDA for Esophageal Stethoscope.
| Device ID | K823703 |
| 510k Number | K823703 |
| Device Name: | ESOPHAGEAL STETHOSCOPE |
| Classification | Stethoscope, Esophageal |
| Applicant | RSP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZW |
| CFR Regulation Number | 868.1910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-09 |
| Decision Date | 1983-01-07 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10695085000730 | K823703 | 000 |