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 K891956
Device Name PATIENT EXAMINATION GLOVE
Applicant
Equatorial Rubber Mfg. Industry Sdn Bhd
Plot 379 & 380 Lorong
Perusahaan 10, Prai Industrial
Estate, 13600 P.W. Penang,  MY
Applicant Contact YEOW CHEEN
Correspondent
Equatorial Rubber Mfg. Industry Sdn Bhd
Plot 379 & 380 Lorong
Perusahaan 10, Prai Industrial
Estate, 13600 P.W. Penang,  MY
Correspondent Contact YEOW CHEEN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/28/1989
Decision Date 05/08/1989
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
-
-