• 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 latex patient examination glove
510(k) Number K891863
Device Name PATIENT EXAM GLOVE (MFG. DALIAN LATEX & JIN ZHOU)
Applicant
CHINA XINXING CORP. LTD.
SHOU SONG HOTEL WAN SHOU ROAD
beijing,  CN
Applicant Contact jing xia
Correspondent
CHINA XINXING CORP. LTD.
SHOU SONG HOTEL WAN SHOU ROAD
beijing,  CN
Correspondent Contact jing xia
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/27/1989
Decision Date 05/31/1989
Decision substantially equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-