The following data is part of a premarket notification filed by Midwest Metabolic Support Group with the FDA for Acessory To Modified Freeding Jejunosto.
| Device ID | K813504 |
| 510k Number | K813504 |
| Device Name: | ACESSORY TO MODIFIED FREEDING JEJUNOSTO |
| Classification | Surgical Instruments, G-u, Manual (and Accessories) |
| Applicant | MIDWEST METABOLIC SUPPORT GROUP 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOA |
| CFR Regulation Number | 876.4730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-15 |
| Decision Date | 1982-01-07 |