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 |