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 K943869
Device Name ULTIMAX (GREEN POWDER FREE EXAMINATION)
Applicant
Wembley Rubber Products (M) Sdn Bhd
84,Jalan Raja Chulan
50200 Kuala Lumpur
Malaysia,  MY
Applicant Contact ONG G CHEE
Correspondent
Wembley Rubber Products (M) Sdn Bhd
84,Jalan Raja Chulan
50200 Kuala Lumpur
Malaysia,  MY
Correspondent Contact ONG G CHEE
Regulation Number880.6250
Classification Product Code
LYY  
Date Received08/08/1994
Decision Date 02/21/1995
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
-
-