Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name saline, vascular access flush
510(k) Number K120836
Device Name 0.9% SODIUM CHLORIDE FLISH SYRINGE
Applicant
AMUSA
5209 Linbar Dr Ste 640
NASHVILLE,  TN  37211
Applicant Contact KAREN THOMISON
Correspondent
AMUSA
5209 Linbar Dr Ste 640
NASHVILLE,  TN  37211
Correspondent Contact KAREN THOMISON
Regulation Number880.5200
Classification Product Code
NGT  
Date Received03/20/2012
Decision Date 07/12/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-