The following data is part of a premarket notification filed by Noble Fiber Technologies with the FDA for Silverseal.
Device ID | K033587 |
510k Number | K033587 |
Device Name: | SILVERSEAL |
Classification | Dressing, Wound, Drug |
Applicant | NOBLE FIBER TECHNOLOGIES 421 S. STATE ST. Clarks Summit, PA 18411 |
Contact | Patricia Davidson |
Correspondent | Patricia Davidson NOBLE FIBER TECHNOLOGIES 421 S. STATE ST. Clarks Summit, PA 18411 |
Product Code | FRO |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2003-11-13 |
Decision Date | 2004-08-05 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SILVERSEAL 90819933 not registered Live/Pending |
SILVERSEAL CORPORATION 2021-07-09 |
SILVERSEAL 81007265 1007265 Dead/Cancelled |
Lee Pharmaceuticals 0000-00-00 |
SILVERSEAL 76465747 2887226 Live/Registered |
NOBLE FIBER TECHNOLOGIES, LLC 2002-11-12 |
SILVERSEAL 73280409 not registered Dead/Abandoned |
GULFKO, INCORPORATED 1980-10-06 |