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 Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
510(k) Number K953805
Device Name 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE
Applicant
ABBOTT LABORATORIES
DEPT. 389, AP30
ABBOTT PARK,  IL  60064 -3537
Applicant Contact THOMAS F WILLER
Correspondent
ABBOTT LABORATORIES
DEPT. 389, AP30
ABBOTT PARK,  IL  60064 -3537
Correspondent Contact THOMAS F WILLER
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received08/08/1995
Decision Date 06/28/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-