The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Leukofix R.
| Device ID | K843873 |
| 510k Number | K843873 |
| Device Name: | LEUKOFIX R |
| Classification | Tape And Bandage, Adhesive |
| Applicant | BEIERSDORF, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KGX |
| CFR Regulation Number | 880.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-02 |
| Decision Date | 1985-02-21 |