The following data is part of a premarket notification filed by Marketing Consultants Of America with the FDA for Tanarama.
| Device ID | K812543 |
| 510k Number | K812543 |
| Device Name: | TANARAMA |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | MARKETING CONSULTANTS OF AMERICA 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-09-04 |
| Decision Date | 1981-10-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TANARAMA 73218560 1156269 Dead/Cancelled |
MARKETING CONSULTANTS OF AMERICA CORPORATION 1979-06-06 |