The following data is part of a premarket notification filed by Radiotherapeutics Corp. with the FDA for Mr Compatible Leveen Needle Electrode.
Device ID | K982854 |
510k Number | K982854 |
Device Name: | MR COMPATIBLE LEVEEN NEEDLE ELECTRODE |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | RADIOTHERAPEUTICS CORP. 2685 MARINE WAY, SUITE 1408 Mountain View, CA 94043 |
Contact | Colin J Nichols |
Correspondent | Colin J Nichols RADIOTHERAPEUTICS CORP. 2685 MARINE WAY, SUITE 1408 Mountain View, CA 94043 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-08-13 |
Decision Date | 1998-11-10 |