The following data is part of a premarket notification filed by Amcad Biomed Corporation with the FDA for Amcad-us.
Device ID | K162574 |
510k Number | K162574 |
Device Name: | AmCAD-US |
Classification | System, Image Processing, Radiological |
Applicant | AmCad BioMed Corporation FL.3, NO. 167, Fu Hsing N. RD. Taipei, TW 105 |
Contact | Jack Yang |
Correspondent | Chiu S. Lin Lin & Associates, LLC 5614 Johnson Avenue Bethesda, MD 20817 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-09-15 |
Decision Date | 2017-05-30 |
Summary: | summary |