The following data is part of a premarket notification filed by Unoplast A/s with the FDA for Vaccon.
Device ID | K896733 |
510k Number | K896733 |
Device Name: | VACCON |
Classification | Tape And Bandage, Adhesive |
Applicant | UNOPLAST A/S DK-3390 HUNDESTED Denmark, DK |
Contact | Erik Andersen |
Correspondent | Erik Andersen UNOPLAST A/S DK-3390 HUNDESTED Denmark, DK |
Product Code | KGX |
CFR Regulation Number | 880.5240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-11-30 |
Decision Date | 1990-02-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VACCON 87497227 5400276 Live/Registered |
Bimba Manufacturing Company 2017-06-20 |