The following data is part of a premarket notification filed by Imm Enterprises Ltd. with the FDA for Cat 10-neurology Device.
| Device ID | K840314 |
| 510k Number | K840314 |
| Device Name: | CAT 10-NEUROLOGY DEVICE |
| Classification | Percussor |
| Applicant | IMM ENTERPRISES LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GWZ |
| CFR Regulation Number | 882.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-24 |
| Decision Date | 1984-02-23 |