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 |