The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Leukopor.
Device ID | K792666 |
510k Number | K792666 |
Device Name: | LEUKOPOR |
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 | 1979-12-27 |
Decision Date | 1980-01-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LEUKOPOR 72241229 0834393 Live/Registered |
P. BEIERSDORF & CO. A.-G. 1966-03-17 |