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 Polymer Patient Examination Glove
510(k) Number K990696
Device Name OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE,WHITE
Applicant
Omnigrace (Thailand) , Ltd.
641 Moo 5 Kanchanawanit Rd.
Tambon Banpru
Hatyai, Songkhla,  TH 90250
Applicant Contact K.C. CHOONG
Correspondent
Omnigrace (Thailand) , Ltd.
641 Moo 5 Kanchanawanit Rd.
Tambon Banpru
Hatyai, Songkhla,  TH 90250
Correspondent Contact K.C. CHOONG
Regulation Number880.6250
Classification Product Code
LZA  
Date Received03/03/1999
Decision Date 05/13/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-