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 Calibrator, Multi-Analyte Mixture
510(k) Number K933955
Device Name DUPONT STANDARD C FOR THE DIMENSION CLINICAL CHEMISTRY SYSTEM
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Bmp22/1170
Wilmington,  DE  19880
Applicant Contact CAROLYN KRUER GEORGE
Correspondent
E.I. Dupont DE Nemours & Co., Inc.
Bmp22/1170
Wilmington,  DE  19880
Correspondent Contact CAROLYN KRUER GEORGE
Regulation Number862.1150
Classification Product Code
JIX  
Date Received08/12/1993
Decision Date 10/13/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-