The following data is part of a premarket notification filed by Amicas, Inc. with the FDA for Amicas Vision Series Pacs, Model 5.5.
Device ID | K073526 |
510k Number | K073526 |
Device Name: | AMICAS VISION SERIES PACS, MODEL 5.5 |
Classification | System, Image Processing, Radiological |
Applicant | AMICAS, INC. 20 GUEST ST. Boston, MA 02135 |
Contact | Patrice Nedelec |
Correspondent | Patrice Nedelec AMICAS, INC. 20 GUEST ST. Boston, MA 02135 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-12-17 |
Decision Date | 2008-03-12 |
Summary: | summary |