The following data is part of a premarket notification filed by Clayton Medical Products, Inc. with the FDA for Tuck-tite Colon Fluid Retainer.
| Device ID | K833860 |
| 510k Number | K833860 |
| Device Name: | TUCK-TITE COLON FLUID RETAINER |
| Classification | Enema Kit |
| Applicant | CLAYTON MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FCE |
| CFR Regulation Number | 876.5210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-07 |
| Decision Date | 1983-12-27 |