Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 blood pressure cuff
510(k) Number K182433
Device Name Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff
Applicant
Shenzhen Caremed Medical Technology Co., Ltd.
East Side, 3/F, C Building, Kelunte Low-Carbon Industries
Gaofeng Community
Dalang Office, Longhua District, Shenzhe,  CN 518109
Applicant Contact Alan Xie
Correspondent
Chonconn Medical Device Consulting Co., Ltd.
No. A415, Block A, Nanshan Medical Devices Industrial Park
Nanshan District
Shenzhen,  CN 518067
Correspondent Contact Kevin Wang
Regulation Number870.1120
Classification Product Code
DXQ  
Date Received09/06/2018
Decision Date 12/17/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-