The following data is part of a premarket notification filed by Vibrant Health with the FDA for Akuport M1.
| Device ID | K020567 |
| 510k Number | K020567 |
| Device Name: | AKUPORT M1 |
| Classification | Device, Galvanic Skin Response Measurement |
| Applicant | VIBRANT HEALTH 150 DES GRANDS COTEAUX Beoeil, Quebec, CA J3g 2c9 |
| Contact | Stephen Emond |
| Correspondent | Stephen Emond VIBRANT HEALTH 150 DES GRANDS COTEAUX Beoeil, Quebec, CA J3g 2c9 |
| Product Code | GZO |
| CFR Regulation Number | 882.1540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-02-20 |
| Decision Date | 2002-05-02 |