Company · CA

Pro-Lab Diagnostics

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1994. 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
LIO	Device, Specimen Collection	4
GMZ	Antigens, All Types, Escherichia Coli	1

Decided	510(k)	Device and applicant	Code
Dec 15, 1994	K944421	E.COLI 0157 LATEX TEST Pro-Lab Diagnostics, CA	GMZ
Dec 24, 1992	K924331	TRANSYSTEM LIQUID STUART MEDIUM Pro-Lab Diagnostics, CA	LIO
Dec 24, 1992	K924330	TRANSYSTEM AMIES WITH CHARCOAL Pro-Lab Diagnostics, CA	LIO
Dec 24, 1992	K924329	TRANSYSTEM AMIES W/O CHARCOAL Pro-Lab Diagnostics, CA	LIO
Dec 24, 1992	K924328	TRANSYSTEM LIQUID AMIES MEDIUM Pro-Lab Diagnostics, CA	LIO

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