• 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
-
31 to 40 of 57 Results
ProductCode: DTQ Decision Date To: 02/26/2017
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
Results per Page
New Search  
Export all 57 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]
modification to stockert s5 system SORIN GROUP DEUTSCHLAND GMBH K062396 09/28/2006
modification to cardiovention powerbase console, model pcb-100 CARDIOVENTION, INC. K030141 02/26/2003
medtronic performer tm cpb, model r51, pcpb RAND S.R.L. K052555 03/15/2006
lifebridge b2t, model 7001 LIFEBRIDGE MEDIZINTECHNIK AG K090006 10/15/2009
jostra hl-20 integrated perfusion system JANUS BIOMEDICAL, INC. K943803 01/30/1996
interface module iddd STOECKERT INSTRUMENTE K992635 12/20/1999
gambro pump console csl GAMBRO, INC. K822068 08/24/1982
essenz hlm, essenz ilbm LivaNova Deutschland GmbH K232291 08/24/2023
essenz hlm LivaNova Deutschland GmbH K221373 03/09/2023
console, mobile for 3 pumps w/masts COBE LABORATORIES, INC. K770002 03/07/1977
-
-