• 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
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]
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
3m brand anesthesia filter,#3110 3M COMPANY K760611 09/21/1976
4-way stopcock w/10 cm exten. tubing AMERICAN VIGGO K760667 12/02/1976
4-way stopcock w/100 cm tubing, luer-lk AMERICAN VIGGO K760678 12/02/1976
4-way stopcock w/7cm tubing, AMERICAN VIGGO K760679 12/02/1976
4-way stopcock w/luer-lock fitting AMERICAN VIGGO K760666 12/02/1976
5m1352 proport. dialysis fluid deliv.ery TRAVENOL LABORATORIES, S.A. K761287 01/03/1977
aca phosphorus analytical test pack E.I. DUPONT DE NEMOURS & CO., INC. K760634 11/24/1976
acid, native-deoxyribonucleic, ivdp ZEUS SCIENTIFIC, INC. K760209 07/26/1976
aggrecetin BIO/DATA CORP. K760893 01/12/1977
airway, dual channel HUDSON OXYGEN THERAPY SALES CO. K760488 09/03/1976

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