CELLONA
Bandage, Cast
SECOL CO.
The following data is part of a premarket notification filed by Secol Co. with the FDA for Cellona.
Pre-market Notification Details
| Device ID | K802792 |
| 510k Number | K802792 |
| Device Name: | CELLONA |
| Classification | Bandage, Cast |
| Applicant | SECOL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ITG |
| CFR Regulation Number | 890.3025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-11-04 |
| Decision Date | 1980-12-10 |
Trademark Results [CELLONA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CELLONA 79012866 3139313 Live/Registered |
Lohmann & Rauscher International GmbH &Co KG 2005-05-06 |
 CELLONA 74456448 1917521 Live/Registered |
LOHMAN & RAUSCHER INTERNATIONAL GMBH & CO. KG 1993-11-04 |
 CELLONA 73025240 1018367 Dead/Expired |
LOHMANN GMBH & CO. KG 1974-06-25 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.