The following data is part of a premarket notification filed by Sectra-imtec Ab with the FDA for Modification To Ids5 Image Display System.
Device ID | K002936 |
510k Number | K002936 |
Device Name: | MODIFICATION TO IDS5 IMAGE DISPLAY SYSTEM |
Classification | System, Image Processing, Radiological |
Applicant | SECTRA-IMTEC AB 2001 EAST OAKSHORES DR. Crossroads, TX 76227 |
Contact | Herman Oosterwijk |
Correspondent | Herman Oosterwijk SECTRA-IMTEC AB 2001 EAST OAKSHORES DR. Crossroads, TX 76227 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-21 |
Decision Date | 2000-10-17 |