The following data is part of a premarket notification filed by Autonomic Equipment Supply Co, with the FDA for Autonorm & Nerv-a-norm.
| Device ID | K811956 |
| 510k Number | K811956 |
| Device Name: | AUTONORM & NERV-A-NORM |
| Classification | Device, Pressure Applying |
| Applicant | AUTONOMIC EQUIPMENT SUPPLY CO, 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNM |
| CFR Regulation Number | 890.5765 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-07-09 |
| Decision Date | 1981-07-31 |