The following data is part of a premarket notification filed by Hologic, Inc. with the FDA for Securview Dx Softcopy Workstation.
Device ID | K041555 |
510k Number | K041555 |
Device Name: | SECURVIEW DX SOFTCOPY WORKSTATION |
Classification | System, Image Processing, Radiological |
Applicant | HOLOGIC, INC. 35 CROSBY DR. Bedford, MA 01730 |
Contact | Richard Follett |
Correspondent | Richard Follett HOLOGIC, INC. 35 CROSBY DR. Bedford, MA 01730 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-06-10 |
Decision Date | 2004-08-09 |
Summary: | summary |