The following data is part of a premarket notification filed by Cilco, Inc. with the FDA for Octopus 500/500e.
| Device ID | K841099 |
| 510k Number | K841099 |
| Device Name: | OCTOPUS 500/500E |
| Classification | Perimeter, Automatic, Ac-powered |
| Applicant | CILCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HPT |
| CFR Regulation Number | 886.1605 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-03-12 |
| Decision Date | 1984-06-19 |