The following data is part of a premarket notification filed by Midwest Metabolic Support Group with the FDA for K-tube Repair Kit.
| Device ID | K840019 |
| 510k Number | K840019 |
| Device Name: | K-TUBE REPAIR KIT |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | MIDWEST METABOLIC SUPPORT GROUP 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-05 |
| Decision Date | 1984-02-10 |