• 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 catheter, continuous flush
510(k) Number K161962
Device Name VAMP Venous/Arterial Blood Management Protection System
Edwards Lifesciences LLC
One Edwards Way
Irvine,  CA  92614
Applicant Contact Jennifer Wilbur
Edwards Lifesciences LLC
One Edwards Way
Irvine,  CA  92614
Correspondent Contact Jennifer Wilbur
Regulation Number870.1210
Classification Product Code
Date Received07/18/2016
Decision Date 11/28/2016
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls