The following data is part of a premarket notification filed by Mavidon Medical Products with the FDA for Mavidon Medical Electrode Jelly.
| Device ID | K003924 |
| 510k Number | K003924 |
| Device Name: | MAVIDON MEDICAL ELECTRODE JELLY |
| Classification | Media, Electroconductive |
| Applicant | MAVIDON MEDICAL PRODUCTS 2105 7TH AVE. NO. Lake Worth, FL 33461 |
| Contact | Tim Carroll |
| Correspondent | Tim Carroll MAVIDON MEDICAL PRODUCTS 2105 7TH AVE. NO. Lake Worth, FL 33461 |
| Product Code | GYB |
| CFR Regulation Number | 882.1275 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-20 |
| Decision Date | 2001-08-24 |