• 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 22 Results
ProductCode: DWF Applicant: DLP, INC Decision Date To: 11/28/2014
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 22 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]
retrograde coronary sinus perfusion cannula with elongated & treaded cuff & introducer stylet DLP, INC. K953945 03/26/1996
catheter two stage venous return DLP, INC. K915268 07/27/1992
code #94315 retrograde coronary sinus perf cannula DLP, INC. K901074 07/06/1990
picso cannula, catalog code 94315 DLP, INC. K897022 03/16/1990
descending arch cannula DLP, INC. K880421 04/28/1988
percutaneous arterial/venous cannula placement kit DLP, INC. K875353 03/22/1988
aspirating needle, catalog code #12006 DLP, INC. K865079 03/03/1987
venous perfusion cannula w/cuff cat. no. 94015 DLP, INC. K860149 03/31/1986
venous return cannula w/cuff 91039 DLP, INC. K854487 02/10/1986
intracardiac sump 12010 DLP, INC. K850385 04/29/1985
-
-