The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Esophageal Motility Tube.
| Device ID | K760761 |
| 510k Number | K760761 |
| Device Name: | ESOPHAGEAL MOTILITY TUBE |
| Classification | System, Gastrointestinal Motility (electrical) |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FFX |
| CFR Regulation Number | 876.1725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-10-04 |
| Decision Date | 1976-11-30 |