• 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
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC | Inspections
 


New Search Back To Search Results
Device Classification Name catheter,intravascular,therapeutic,short-term less than 30 days
510(k) Number K032417
Device Name HEPARIN LOCK FLUSH SYRINGE
Original Applicant
AM2 PAT INC.
9400 ransdell rd., suite 10
raleigh,  NC  27603
Original Contact dushyant patel
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received08/05/2003
Decision Date 12/23/2003
Decision substantially equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-