• 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 500 Results *
Decision Date To: 07/22/2019
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 500 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]
zzoma positional sleeper model 001 SLEEP SPECIALISTS, LLC K100160 05/11/2010
zzipp instant bovie cleaner GRIESHABER & CO. K900714 03/27/1990
zywieai software library Zywie, Inc. K142693 02/20/2015
zytron PREMIER DENTAL PRODUCTS CO. K780796 06/22/1978
zyto hand cradle ZYTO TECHNOLOGIES, INC K111308 08/30/2011
zyston strut open titanium spacer system Zimmer Biomet Spine Inc. K171495 02/12/2018
zyston straight spacer system BIOMET SPINE K112014 10/17/2011
zyston arc interbody spacer BIOMET SPINE (AKA EBI, LLC) K110650 06/30/2011
zyranox zirconia ceramic femoral heads CORIN U.S.A. K992235 11/23/1999
zyppah anti-snoring device Always More Marketing K182312 01/24/2019

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
-
-