TRICOPLAST
Tape And Bandage, Adhesive
BEIERSDORF, INC.
The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Tricoplast.
Pre-market Notification Details
| 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 |
Trademark Results [TRICOPLAST]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TRICOPLAST 74157442 not registered Dead/Abandoned |
BEIERSDORF AKTIENGESELLSCHAFT 1991-03-28 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.