The following data is part of a premarket notification filed by Secol Co. with the FDA for Solvaline.
| Device ID | K802790 |
| 510k Number | K802790 |
| Device Name: | SOLVALINE |
| Classification | Drape, Surgical |
| Applicant | SECOL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-11-04 |
| Decision Date | 1981-02-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOLVALINE 76362147 3072383 Dead/Cancelled |
Lohmann & Rauscher International GmbH &Co. KG 2002-01-23 |