The following data is part of a premarket notification filed by Light Sources, Inc. with the FDA for U.v. Sunlamp (u.v. Light, Dermatologic).
| Device ID | K900693 |
| 510k Number | K900693 |
| Device Name: | U.V. SUNLAMP (U.V. LIGHT, DERMATOLOGIC) |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | LIGHT SOURCES, INC. P.O. BOX 569 410 MAIN ST. Ansonia, CT 06401 |
| Contact | Gene Czako |
| Correspondent | Gene Czako LIGHT SOURCES, INC. P.O. BOX 569 410 MAIN ST. Ansonia, CT 06401 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-13 |
| Decision Date | 1990-03-27 |