The following data is part of a premarket notification filed by Ethox Corp. with the FDA for Ehtox Gastric Lavage Kit #2050 & #2070.
| Device ID | K812648 |
| 510k Number | K812648 |
| Device Name: | EHTOX GASTRIC LAVAGE KIT #2050 & #2070 |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | ETHOX CORP. 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 | 1981-09-17 |
| Decision Date | 1981-09-29 |