The following data is part of a premarket notification filed by Cilco, Inc. with the FDA for K-sol.
| Device ID | K844249 |
| 510k Number | K844249 |
| Device Name: | K-SOL |
| Classification | Media, Corneal Storage |
| Applicant | CILCO, INC. 1616 13TH. AVE. SUITE 200 Huntington, WV 25701 |
| Contact | Rich Mccarley |
| Correspondent | Rich Mccarley CILCO, INC. 1616 13TH. AVE. SUITE 200 Huntington, WV 25701 |
| Product Code | LYX |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-11-02 |
| Decision Date | 1985-04-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() K-SOL 86471394 4833591 Live/Registered |
Laser Pharmaceuticals, LLC 2014-12-04 |
![]() K-SOL 75118352 not registered Dead/Abandoned |
GIVAUDAN-ROURE (International) S.A. 1996-06-13 |
![]() K-SOL 73631081 1471923 Dead/Cancelled |
CILCO, INC. 1986-11-19 |