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 negative pressure wound therapy powered suction pump
510(k) Number K123878
Device Name PREVENA INCISION MANAGEMENT SYSTEM WITH CUSTOMIZABLE DRESSING
Applicant
KCI USA, INC. (KINETIC CONCEPTS, INC.)
6203 FARINON DRIVE
SAN ANTONIO,  TX  78249
Applicant Contact Shannon Scott
Correspondent
KCI USA, INC. (KINETIC CONCEPTS, INC.)
6203 FARINON DRIVE
SAN ANTONIO,  TX  78249
Correspondent Contact Shannon Scott
Regulation Number878.4780
Classification Product Code
OMP  
Date Received12/17/2012
Decision Date 01/15/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-