• 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 K892994
Device Name NON-STERILE VINYL EXAMINATION GLOVES
Applicant
SIAN-YU INDUSTRIAL CO., LTD.
P.O. BOX 878
HAZLEHURST,  MS  39083
Applicant Contact WILLIAM LOWENKAMP,JR
Correspondent
SIAN-YU INDUSTRIAL CO., LTD.
P.O. BOX 878
HAZLEHURST,  MS  39083
Correspondent Contact WILLIAM LOWENKAMP,JR
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received04/12/1989
Decision Date 09/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-