Company · US

Techlab Inc., Corporate Research Center

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2012. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GMZ	Antigens, All Types, Escherichia Coli	2
DEG	Lactoferrin, Antigen, Antiserum, Control	1
MHI	Giardia Spp.	1
NBT	Antibodies, Saccharomyces Cerevisiae (S.Cerevisiae)	1

Decided	510(k)	Device and applicant	Code
Oct 2, 2012	K121411	SHIGA TOXIN CHEK Techlab Inc., Corporate Research Center	GMZ
Oct 2, 2012	K121364	SHIGA TOXIN QUIK CHEK Techlab Inc., Corporate Research Center	GMZ
Aug 18, 2011	K103673	GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK Techlab Inc., Corporate Research Center	MHI
Dec 4, 2007	K071712	LEUKO EZ VUE Techlab Inc., Corporate Research Center	DEG
Nov 7, 2007	K071711	ASCA-CHEK Techlab Inc., Corporate Research Center	NBT

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.