FDA 510(k) Applications Submitted by DEBORAH L MORRIS

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
K071017	04/10/2007	IMMULITE 2500 HIGH SENSITIVITY C-REACTIVE PROTEIN, MODELS L5KCRP (200 TESTS), L5KCRP (600 TESTS)	SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS
K063045	10/04/2006	IMMULITE 2000, IMMULITE 2500 VANCOMYCIN	DIAGNOSTIC PRODUCTS CORP.
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