The following data is part of a premarket notification filed by Michael R. Kiss with the FDA for Electrostimuli Aversion Machine.
| Device ID | K820622 |
| 510k Number | K820622 |
| Device Name: | ELECTROSTIMULI AVERSION MACHINE |
| Classification | Device, Aversive Conditioning |
| Applicant | MICHAEL R. KISS 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 | 1982-03-08 |
| Decision Date | 1982-04-09 |