• 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 Vinyl Patient Examination Glove
510(k) Number K992017
Device Name DISPOSABLE PVC SYNTHETIC EXAMINATION GLOVES, POWDER FREE
Applicant
SHANGHAI ANTARES INDUSTRIES, INC.
259 YUSHU RD.,
CANGQIAO TOWNSHIP
SONGJIANG SHANGHAI,  CN
Applicant Contact JOHN LAI
Correspondent
SHANGHAI ANTARES INDUSTRIES, INC.
259 YUSHU RD.,
CANGQIAO TOWNSHIP
SONGJIANG SHANGHAI,  CN
Correspondent Contact JOHN LAI
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received06/15/1999
Decision Date 08/05/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-