• 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
-
21 to 25 of 25 Results
ProductCode: DQK Applicant: GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES Decision Date To: 05/20/2022
 < 
 1 
 2 
 3 
 
Results per Page
New Search  
Export all 25 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]
graffiti GE Medical Systems Information Technologies, Inc. K202189 12/08/2020
case cardiac testing system, cs cardiac testing system GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH K103678 02/16/2011
carescape one and carescape dock f0, model numbers mbz323 and mfa101, carescape ecg, model number mke101,carescape temp, model number mkt101, carescape pres, model number mkp101, carescape spo2, model numbers mks101 and mks201 GE Medical Systems Information Technologies, Inc. K213234 04/12/2022
cardiosoft/case cardiac testing system GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES K031561 08/01/2003
capnostat / capnoflex co2 system GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES K083750 03/23/2009
-
-