The following data is part of a premarket notification filed by Williams & Connolly with the FDA for Sunlamp.
| Device ID | K811029 |
| 510k Number | K811029 |
| Device Name: | SUNLAMP |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | WILLIAMS & CONNOLLY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-16 |
| Decision Date | 1981-06-02 |