FDA 510(k) Applications Submitted by DIAGNOSTIC PRODUCTS CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K060929 04/05/2006 IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6 DIAGNOSTIC PRODUCTS CORPORATION
K063057 10/05/2006 IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP DIAGNOSTIC PRODUCTS CORPORATION
K053533 12/19/2005 IMMULITE/IMMULITE 1000 TURBO INTACT PTH DIAGNOSTIC PRODUCTS CORPORATION


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