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 K892622
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Latexon Co., Ltd.
Suite 2500
1225 Seventeenth St.
Denver,  CO  80202
Applicant Contact CHARLES J FRIEDMAN
Correspondent
Latexon Co., Ltd.
Suite 2500
1225 Seventeenth St.
Denver,  CO  80202
Correspondent Contact CHARLES J FRIEDMAN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/10/1989
Decision Date 09/07/1989
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
-
-