FDA 510(k) Applications Submitted by Robert Di Tullio

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180041	01/05/2018	BioCode Gastrointestinal Pathogen Panel (GPP)	Applied Biocode, Inc.
K190585	03/06/2019	Biocode Gastrointestinal Pathogen Panel (GPP)	Applied Biocode, Inc.
K192485	09/10/2019	BioCode Respiratory Pathogen Panel (RPP)	Applied BioCode, Inc.
K970227	01/17/1997	IMMULITE 2000 AUTOMATED IMMUNOASSAY ANALYZER	DPC CIRRUS
K980855	03/05/1998	IMMULITE 2000 CARCINOEMBRYONIC ANTIGEN (CEA) KIT	DPC CIRRUS
K021206	04/16/2002	IMMULITE 2000 SPECIFIC ALLERGENS	DIAGNOSTIC PRODUCTS CORP.
K021208	04/16/2002	IMMULITE 2000 MIXED ALLERGEN PANELS	DIAGNOSTIC PRODUCTS CORP.
K974842	12/24/1997	IMMULITE 2000 3RD GENERATION PSA	DIAGNOSTIC PRODUCTS CORP.
K972095	06/04/1997	IMMULITE 2000 PSA	DIAGNOSTIC PRODUCTS CORP.