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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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