• 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 Surgeon'S Gloves
510(k) Number K151607
Device Name Finessis Zero Flexylon Powder Free Sterile White Surgical Glove
Applicant
Lucenxia Prescience AG
Rathautrasse 7
Baar,  CH 6341
Applicant Contact Robert Hill
Correspondent
Lucenxia Prescience AG
Rathautrasse 7
Baar,  CH 6341
Correspondent Contact Robert Hill
Regulation Number878.4460
Classification Product Code
KGO  
Date Received06/15/2015
Decision Date 11/16/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-