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 Latex Patient Examination Glove
510(k) Number K021465
Device Name MIDAS TOUCH LATEX EXAMINATION GLOVES-POLYMER COATED, POWDER FREE
Applicant
INDUSTRIAL CLOTHINGS, LTD.
481A, PRINCE OF WALES AVE.
COLOMBO 14,  LK
Applicant Contact UMAIR AHMED
Correspondent
INDUSTRIAL CLOTHINGS, LTD.
481A, PRINCE OF WALES AVE.
COLOMBO 14,  LK
Correspondent Contact UMAIR AHMED
Regulation Number880.6250
Classification Product Code
LYY  
Date Received05/07/2002
Decision Date 05/22/2002
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
-
-