Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Euro-Diagnostica AB

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K093908	CCPOINT	NHX	2010-12-01	View
510(k)	K091657	IMMUNOSCAN CCPLUS	NHX	2009-11-19	View
510(k)	K062045	EDIA ANTI-CCP	NHX	2006-12-04	View
510(k)	K971689	IMMUNOSCAN ANTI-MYELOPEROXIDASE ANTIBODIES (MPO-ANCA) QUANTITATIVE KIT	MOB	1997-10-29	View
510(k)	K971464	IMMUNOSCAN ANTI-GBM QUANTITATIVE KIT	DBL	1997-10-29	View
510(k)	K971690	IMMUNOSCAN PR3-ANCA	MOB	1997-10-29	View

↑