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Company · US

U.S. Drug Testing, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 1994. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
DIO	Enzyme Immunoassay, Cocaine And Cocaine Metabolites	1
DJG	Enzyme Immunoassay, Opiates	1
DKZ	Enzyme Immunoassay, Amphetamine	1
KZR	Chromatography (Liquid, Gel), Clinical Use	1
LCM	Enzyme Immunoassay, Phencyclidine	1
LDJ	Enzyme Immunoassay, Cannabinoids	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jun 2, 1994	K940912	USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 U.S. Drug Testing, Inc.	LDJ
Apr 12, 1994	K935629	USDT PHENCYCLIDINE (PCP) ASSAY COLUMN CAT. NO. 9000-400 U.S. Drug Testing, Inc.	LCM
Nov 22, 1993	K934693	AMPHETAMINE TEST SYSTEM U.S. Drug Testing, Inc.	DKZ
Jun 15, 1993	K932318	USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 U.S. Drug Testing, Inc.	DJG
May 6, 1993	K931227	USDT FLOW IMMUNOASSAY SYSTEM, MODEL 9000 U.S. Drug Testing, Inc.	KZR
Apr 27, 1993	K930985	USDT COCAINE/COCAINE METABOL ASSAY COLUMN,9000-100 U.S. Drug Testing, Inc.	DIO

Latest recalls

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

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