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 K892043
Device Name PATIENT EXAMINATION GLOVE (LATEX)
Applicant
Mwe Asia America Industries Sdn
47400 Petaling
Selangor,  MY
Applicant Contact SEONG LYE
Correspondent
Mwe Asia America Industries Sdn
47400 Petaling
Selangor,  MY
Correspondent Contact SEONG LYE
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/31/1989
Decision Date 08/23/1989
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
-
-