The following data is part of a premarket notification filed by Eckert & Ziegler Bebig Gmbh with the FDA for Saginova.
| Device ID | K142986 |
| 510k Number | K142986 |
| Device Name: | SagiNova |
| Classification | System, Applicator, Radionuclide, Remote-controlled |
| Applicant | Eckert & Ziegler BEBIG GmbH Robert-Rossie-Str. 10 Berlin, DE 13125 |
| Contact | Michel Lafuente |
| Correspondent | Lu Anne Johnson Capamed Inc. 1917 29 3/4 Ave Rice Lake, WI 54868 |
| Product Code | JAQ |
| CFR Regulation Number | 892.5700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-10-16 |
| Decision Date | 2015-04-17 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SAGINOVA 79125749 4452972 Live/Registered |
Eckert & Ziegler BEBIG GmbH 2012-12-04 |