The following data is part of a premarket notification filed by Jackson Ent. with the FDA for Habitsabater.
| Device ID | K790738 |
| 510k Number | K790738 |
| Device Name: | HABITSABATER |
| Classification | Device, Aversive Conditioning |
| Applicant | JACKSON ENT. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HCB |
| CFR Regulation Number | 882.5235 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-16 |
| Decision Date | 1979-06-20 |