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 |