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 K935699
Device Name COLORED POWDER FREE PATIENT EXAMINATION GLOVES
Applicant
Glove India Private , Ltd.
12019 Park River Dr.
Manassas,  VA  22111
Applicant Contact MEHUL RANDERY
Correspondent
Glove India Private , Ltd.
12019 Park River Dr.
Manassas,  VA  22111
Correspondent Contact MEHUL RANDERY
Regulation Number880.6250
Classification Product Code
LYY  
Date Received11/30/1993
Decision Date 02/03/1994
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
-
-