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 |