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.

Techlab Inc., Corporate Research Center

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K121364	SHIGA TOXIN QUIK CHEK	GMZ	2012-10-02	View
510(k)	K121411	SHIGA TOXIN CHEK	GMZ	2012-10-02	View
510(k)	K103673	GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK	MHI	2011-08-18	View
510(k)	K071712	LEUKO EZ VUE	DEG	2007-12-04	View
510(k)	K071711	ASCA-CHEK	NBT	2007-11-07	View

↑