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 Pump, Infusion
510(k) Number K873776
Device Name IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+
Applicant
Y
P.O. BOX 85335
SAN DIEGO,  CA  92138 -5335
Applicant Contact ROBERT J BARD
Correspondent
Y
P.O. BOX 85335
SAN DIEGO,  CA  92138 -5335
Correspondent Contact ROBERT J BARD
Regulation Number880.5725
Classification Product Code
FRN  
Date Received09/16/1987
Decision Date 12/03/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-