The following data is part of a premarket notification filed by Dynatronics Corp. with the FDA for Dynatron 525.
| Device ID | K961261 |
| 510k Number | K961261 |
| Device Name: | DYNATRON 525 |
| Classification | Interferential Current Therapy |
| Applicant | DYNATRONICS CORP. 7030 PARK CENTRE DR. Salt Lake City, UT 84121 |
| Contact | John S Ramey |
| Correspondent | John S Ramey DYNATRONICS CORP. 7030 PARK CENTRE DR. Salt Lake City, UT 84121 |
| Product Code | LIH |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-02 |
| Decision Date | 1996-09-05 |