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 Stand, Infusion
510(k) Number K864753
Device Name FREE SPIRIT(TM) I.V. STAND
Applicant
Demstar Corp.
C/O Lindquist & Vennum
4200 Ids Center
Minneapolis,  MN  55402
Applicant Contact RICHARD D MCNEIL
Correspondent
Demstar Corp.
C/O Lindquist & Vennum
4200 Ids Center
Minneapolis,  MN  55402
Correspondent Contact RICHARD D MCNEIL
Regulation Number880.6990
Classification Product Code
FOX  
Date Received12/05/1986
Decision Date 01/20/1987
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
-
-