Microline Screen for Barbiturates

FDA 510(k) K933480 · Drug Screening Systems, Inc.

Substantially Equivalent

510(k) numberK933480

Submission

Device name
Microline Screen for Barbiturates
Applicant
Drug Screening Systems, Inc.
Blackwood, NJ, US
Received
July 15, 1993
Decision date
October 29, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DIS – Enzyme Immunoassay, Barbiturate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3150
Specialty
Clinical Toxicology

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More from Phamatech, Inc.

510(k)DeviceDecision
K945829Microline Screen for BenzodiazepineJXM · Traditional 01/25/1995SE
K935052Microline Screen for AmphetamineDKZ · Traditional 09/16/1994SE
K921651Microline Screen for PhencyclidineLCM · Traditional 07/08/1992SE
K914915Microline Screen for CannabinoidLDJ · Traditional 01/22/1992SE
K911652Mircoline Screen for CocaineDIO · Traditional 05/15/1991SE
K910525Microline Screen for MethamphetamineDIT · Traditional 04/05/1991SE
K905491Microline Screen for OpiatesDJG · Traditional 03/13/1991SE

Questions and answers

When was Microline Screen for Barbiturates cleared by the FDA?

Microline Screen for Barbiturates (K933480) received a 510(k) decision of Substantially Equivalent on October 29, 1993, 106 days after the submission was received.

What is the product code of K933480?

The FDA product code is DIS – Enzyme Immunoassay, Barbiturate, a Class II (moderate risk) device regulated under 21 CFR 862.3150.