The following data is part of a premarket notification filed by Elekta Instrument Ab with the FDA for Leksell Gamma Knife Icon.
Device ID | K151561 |
510k Number | K151561 |
Device Name: | Leksell Gamma Knife Icon |
Classification | System, Radiation Therapy, Radionuclide |
Applicant | ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18 Stockholm, SE 10393 |
Contact | Matilda Forsberg |
Correspondent | Matilda Forsberg ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18 Stockholm, SE 10393 |
Product Code | IWB |
CFR Regulation Number | 892.5750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-10 |
Decision Date | 2015-08-04 |
Summary: | summary |