• 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 16 Results
ProductCode: GEI Applicant: AESCULAP, INC. Decision Date To: 04/18/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 16 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]
caiman 5 maryland Aesculap, Inc. K183180 03/12/2019
caiman seal and cut technology Aesculap, Inc. K151858 07/21/2015
caiman seal and cut technology AESCULAP, INC. K151696 07/20/2015
caiman seal and cut technology AESCULAP, INC. K140839 04/28/2014
caiman seal and cut technology AESCULAP, INC. K130596 03/22/2013
bipolar hf device AESCULAP, INC. K110695 06/28/2011
reposable instrument system, models mf001-mf083 AESCULAP, INC. K014207 03/21/2002
nelson electrosurgical unit, model gn640 AESCULAP, INC. K014172 03/19/2002
bipolar irrigation forceps AESCULAP, INC. K012986 10/03/2001
sovereign bipolar instruments AESCULAP, INC. K001330 05/30/2000
-
-