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 Polymer Patient Examination Glove
510(k) Number K210755
Device Name Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Blue)
Applicant
Meditech Gloves Sdn Bhd
Pt 3345, Jalan Permata 1/3, Arab Malaysian Industrial Park
Nilai,  MY 71800
Applicant Contact Effendi Tenang
Correspondent
Meditech Gloves Sdn Bhd
Pt 3345, Jalan Permata 1/3, Arab Malaysian Industrial Park
Nilai,  MY 71800
Correspondent Contact Wan Nadzifah Wan Hassan
Regulation Number880.6250
Classification Product Code
LZA  
Date Received03/15/2021
Decision Date 05/07/2021
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-