Dynatronics Laser Corp. · Class II · Cleared Oct 4, 1990
| K-number | K900639 |
| Device name | DYNATRON 350 EMG/BIOFEEDBACK ANALYZER |
| Applicant | Dynatronics Laser Corp. |
| Product code | HCC |
| Device class | Class II |
| Decision date | Oct 4, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 882.5050 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov