• 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 calibrator, multi-analyte mixture
510(k) Number K062334
Device Name DIMENSION VISTA CHEMISTRY 3 CALIBRATOR, MODEL KC130
Applicant
DADE BEHRING, INC.
P.O. BOX BOX 6101, M/S 514
NEWARK,  DE  19714 -6101
Applicant Contact VICTOR M CARRIO
Correspondent
DADE BEHRING, INC.
P.O. BOX BOX 6101, M/S 514
NEWARK,  DE  19714 -6101
Correspondent Contact VICTOR M CARRIO
Regulation Number862.1150
Classification Product Code
JIX  
Date Received08/10/2006
Decision Date 09/22/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-