• 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 K893100
Device Name VINYL EXAMINATION GLOVES
Applicant
Tong Shiung Plastics Industry
20275 Paseo Del Prado
Walnut,  CA  91789
Applicant Contact SHAWN LIN
Correspondent
Tong Shiung Plastics Industry
20275 Paseo Del Prado
Walnut,  CA  91789
Correspondent Contact SHAWN LIN
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received04/14/1989
Decision Date 09/11/1989
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
-
-