The following data is part of a premarket notification filed by Durham Electric Co. with the FDA for Electrical Vibrating Device.
| Device ID | K821133 |
| 510k Number | K821133 |
| Device Name: | ELECTRICAL VIBRATING DEVICE |
| Classification | Vibrator, Therapeutic |
| Applicant | DURHAM ELECTRIC CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IRO |
| CFR Regulation Number | 890.5975 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-20 |
| Decision Date | 1982-07-09 |