• 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 negative pressure wound therapy powered suction pump
510(k) Number K160451
Device Name V. A.C. VeraFlo Cleanse Choice Dressing System for use with the V.A.C. Ulta ...
Applicant
KCI USA, INC. (KINETIC CONCEPTS, INC.)
6203 FARINON DRIVE
san antonio,  TX  78249
Applicant Contact melanie avila
Correspondent
KCI USA, INC.
6203 FARINON DRIVE
san antonio,  TX  78249
Correspondent Contact melanie avila
Regulation Number878.4780
Classification Product Code
OMP  
Date Received02/18/2016
Decision Date 06/20/2016
Decision substantially equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-