• 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
-
121 to 130 of 219 Results
ProductCode: ngx Decision Date To: 05/21/2022
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
Results per Page
New Search  
Export all 219 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]
legend pro dma Pollogen, Ltd K200545 10/21/2021
katalyst training system Katalyst Inc. K190966 02/03/2020
katalyst mark 1 muscle stimulation system model 2 Katalyst Inc. K181199 09/20/2018
katalyst mark 1 muscle stimulation system Katalyst Inc. K171035 09/06/2017
jkh stimulator plus JKH USA, LLC K182203 03/14/2019
jkh stimulator plus JKH USA, LLC K191151 06/21/2019
iq technologies IQ Technologies Inc. K170659 05/26/2017
iq technologies IQ TECHNOLOGIES INC. K131290 08/06/2014
ion magnum genius ION GENIUS INC K123158 06/21/2013
intrelief EasyMed Instruments Co., Ltd. K211263 12/30/2021
-
-