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 set, administration, intravascular
510(k) Number K852881
Device Name VENTED SECONDARY IV ADMINISTRATION SET
Applicant
LYPHOMED, INC.
2045 NORTH CORNELL AVE.
MELROSE PARK,  IL  60160
Applicant Contact DIANE M KOMOS
Correspondent
LYPHOMED, INC.
2045 NORTH CORNELL AVE.
MELROSE PARK,  IL  60160
Correspondent Contact DIANE M KOMOS
Regulation Number880.5440
Classification Product Code
FPA  
Date Received07/09/1985
Decision Date 08/16/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-