The following data is part of a premarket notification filed by Radionics, Inc. with the FDA for Radionics Slice Editor Imaging Software Utility.
Device ID | K981597 |
510k Number | K981597 |
Device Name: | RADIONICS SLICE EDITOR IMAGING SOFTWARE UTILITY |
Classification | Accelerator, Linear, Medical |
Applicant | RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
Contact | Lisa Misterka Benati |
Correspondent | Lisa Misterka Benati RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-05-04 |
Decision Date | 1998-10-09 |
Summary: | summary |