• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name display, diagnostic radiology
510(k) Number K172815
Device Name 2MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)
Applicant
Shenzhen Beacon Display Technology Co., Ltd.
12F, Block B1, Nanshan Zhiyuan, No.1001 Xueyuan Road
Shenzhen,  CN 518055
Applicant Contact Fu Ailing
Correspondent
Shenzhen Beacon Display Technology Co., Ltd.
12F, Block B1, Nanshan Zhiyuan, No.1001 Xueyuan Road
Shenzhen,  CN 518055
Correspondent Contact Fu Ailing
Regulation Number892.2050
Classification Product Code
PGY  
Date Received09/18/2017
Decision Date 10/27/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-