The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Tricoplast.
Device ID | K921760 |
510k Number | K921760 |
Device Name: | TRICOPLAST |
Classification | Tape And Bandage, Adhesive |
Applicant | BEIERSDORF, INC. 360 MARTIN LUTHER KING DR. P.O. BOX 5529 Norwalk, CT 06856 |
Contact | Kenneth M Nicoll |
Correspondent | Kenneth M Nicoll BEIERSDORF, INC. 360 MARTIN LUTHER KING DR. P.O. BOX 5529 Norwalk, CT 06856 |
Product Code | KGX |
CFR Regulation Number | 880.5240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-04-14 |
Decision Date | 1992-08-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRICOPLAST 74157442 not registered Dead/Abandoned |
BEIERSDORF AKTIENGESELLSCHAFT 1991-03-28 |