The following data is part of a premarket notification filed by Wide Corporation with the FDA for Mw100 (mammography) Lcd Monitor System.
Device ID | K110596 |
510k Number | K110596 |
Device Name: | MW100 (MAMMOGRAPHY) LCD MONITOR SYSTEM |
Classification | System, Image Processing, Radiological |
Applicant | WIDE CORPORATION 1600 MANCHESTER WAY Corinth, TX 76210 |
Contact | Carl Alletto |
Correspondent | Carl Alletto WIDE CORPORATION 1600 MANCHESTER WAY Corinth, TX 76210 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-03-02 |
Decision Date | 2011-11-18 |
Summary: | summary |