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
-
1 to 10 of 17 Results
ProductCode: MKJ Applicant: CARDIAC SCIENCE Decision Date To: 02/26/2021
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 17 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
powerheart g5 aed CARDIAC SCIENCE CORPORATION K143714 05/04/2015
powerheart g5 aed CARDIAC SCIENCE CORPORATION K122758 02/12/2014
powerheart aed g3 semi-automatic, powerheart aed g3 automatic, powerheart aed g3 pro, powerheart aed g3 plus CARDIAC SCIENCE CORPORATION K102496 06/09/2011
powerheart aed g3, model 9390e, powerheart aed g3 automatic, model 9390a CARDIAC SCIENCE CORPORATION K091943 09/10/2009
9131 defibrillation electrodes CARDIAC SCIENCE CORPORATION K082090 12/12/2008
modification to powerheart ecd CARDIAC SCIENCE CORPORATION K060934 05/15/2006
powerheart ecd CARDIAC SCIENCE, INC. K052316 01/03/2006
powerheart aed g3 (model 9390e), powerheart aed g3 automatic (model 9390a) CARDIAC SCIENCE, INC. K052161 10/21/2005
powerheart aed g3 pro CARDIAC SCIENCE, INC. K040637 08/06/2004
powerheart aed g3a CARDIAC SCIENCE, INC. K040438 07/01/2004
-
-