QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE— 510(k) K990325

Name: FDA 510(k) clearance K990325
Creator: U.S. Food and Drug Administration
Published: 1999-06-24

Substantially Equivalent

Syntron Bioresearch, Inc.

FDA 510(k) clearance K990325 for QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE, Substantially Equivalent on 1999-06-24. Applicant: Syntron Bioresearch, Inc.. Device class: 2.

Clearance details

Applicant: Syntron Bioresearch, Inc.
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1999-02-02
Decision date: 1999-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Simi Valley, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DKZ

view all

K240670 — DRI Ecstasy Plus Assay2024-10-30
K233019 — AllTest Multi-Drug Rapid Test Cup +3 more2023-12-13
K231137 — Xenta Drug Screen Cup, Xenta Drug Screen Dipcard2023-05-19
K200363 — Quidel Triage® TOX Drug Screen, 946002020-03-11
K191099 — Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test Panel2019-10-03

More clearances from Syntron Bioresearch, Inc.

view all

K993490 — QUICKSTRIP ONE STEP OPIATES TEST1999-10-29
K993491 — QUICKPAC II ONE STEP OPIATES TEST1999-10-29
K992990 — QUICKPAC II ONE STEP COCAINE TEST1999-09-20
K992748 — DRUGCHECK X MULTIDRUG SCREENING DEVICE1999-09-02
K992207 — QUIKSTRIP ONE STEP COCAINE ASSAY (COCAINE AND COCAINE METABOLITE TEST SYSTEM1999-07-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.