The following data is part of a premarket notification filed by Selomas, Inc. with the FDA for Vitasan.
Device ID | K821259 |
510k Number | K821259 |
Device Name: | VITASAN |
Classification | Stocking, Medical Support (for General Medical Purposes) |
Applicant | SELOMAS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FQL |
CFR Regulation Number | 880.5780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-04-30 |
Decision Date | 1982-06-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VITASAN 79105813 4277699 Live/Registered |
"GECCO" Import-Export Handelsgesellschaft m.b.H. 2011-07-25 |
VITASAN 75439111 not registered Dead/Abandoned |
FABER & CO LTD. 1998-02-23 |
VITASAN 73427958 1335341 Dead/Cancelled |
Pardes Spezialstrumpfe GmbH & Co. KG 1983-05-27 |