• 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
-
81 to 90 of 251 Results
ProductCode: ngx Decision Date To: 01/23/2017
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
Results per Page
New Search  
Export all 251 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]
slendertone connect abs BIO-MEDICAL RESEARCH LTD. K151903 11/06/2015
hi-dow wireless tens/ems system (model hd-sn) Hi-Dow International, Inc. K163393 08/04/2017
slendertone® connect abs, type 570 Bio-Medical Research Ltd. K161974 11/01/2016
pain therapy device Guangzhou Xinbo Electronic Co., Ltd. K163611 09/19/2017
smart pain reliever, model lt5019 SHENZHEN DONGDIXIN TECHNOLOGY CO., LTD. K162479 02/08/2017
cur model 1 Thimble Bioelectronics, Inc. K160052 05/20/2016
well life wireless tens/ems stimulator, models wr-2605/2605a WELL-LIFE HEALTHCARE LIMITED K161453 12/05/2016
am-100 BTL INDUSTRIES, INC K163165 02/16/2017
everyway otc ems, model ev-805 EVERYWAY MEDICAL INSTRUMENT CO., LTD. K162744 08/03/2017
electronic pulse stimulator model: pl-029k12 and pl-029k13 JKH Health Co., Ltd. K162517 04/14/2017
-
-