The following data is part of a premarket notification filed by Jay-mar International Enterprises, In with the FDA for Figuretrim.
| Device ID | K780730 |
| 510k Number | K780730 |
| Device Name: | FIGURETRIM |
| Classification | Stimulator, Muscle, Diagnostic |
| Applicant | JAY-MAR INTERNATIONAL ENTERPRISES, IN 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ISB |
| CFR Regulation Number | 890.1850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-05-02 |
| Decision Date | 1978-05-09 |