The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Tube, Feeding, Argyle.
| Device ID | K760137 |
| 510k Number | K760137 |
| Device Name: | TUBE, FEEDING, ARGYLE |
| Classification | Tube, Feeding |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPD |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-28 |
| Decision Date | 1976-07-16 |