The following data is part of a premarket notification filed by Secol Co. with the FDA for Cellamin.
| Device ID | K802796 |
| 510k Number | K802796 |
| Device Name: | CELLAMIN |
| 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 | 1980-11-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CELLAMIN 73334568 1250136 Dead/Cancelled |
Lohmann GmbH & Co. KG 1981-10-28 |