510(k) Report

510(k) · Cleared

Cleared

Psychemedics Cannabinoids Eia

K111929510(k) TraditionalCleared May 1, 2012300-day reviewClass II21 CFR 862.3870

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Psychemedics Corp. · LDJ Enzyme Immunoassay, Cannabinoids

Cleared on May 1, 2012 as substantially equivalent to K011426 (Psychemedics Corp., 2002) after a 300-day review. Its family tree reaches back 1 generation to 2002. 1 later device descends from it.

Decided
May 1, 2012
Review
300 days
Class
Class II
Product code
LDJ
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K011426 (2002). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2012: 1 descendant clearedK011426 · Psychemedics Ria Cannabinoid Assay · Psychemedics Corp. · 2002200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant K011426 · Psychemedics Ria Cannabinoid Assay · Psychemedics Corp. · 20020
  1. Root · 1 generation backK011426 Psychemedics Ria Cannabinoid AssayPsychemedics Corp. · 2002
  2. This deviceK111929 Psychemedics Cannabinoids EiaPsychemedics Corp. · 2012
  3. Descendant · cites it directly · 0 of its ownK122759 Omega Laboratories Hair Drug Screening Assay Cardoxy-THC (Thca)Omega Laboratories, Inc. · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K122759Omega Laboratories Hair Drug Screening Assay Cardoxy-THC (Thca)Omega Laboratories, Inc. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K011426Psychemedics Ria Cannabinoid AssayPsychemedics Corp.2002—
0 (this device)K111929Psychemedics Cannabinoids EiaPsychemedics Corp.2012—
+1K122759Omega Laboratories Hair Drug Screening Assay Cardoxy-THC (Thca)Omega Laboratories, Inc.2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K111929, 2002–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LDJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LDJ device

  1. #1 K232732 Rapid Marijuana (THC) Test Strip 20, Rapid…score 9.4 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K011426Psychemedics Ria Cannabinoid Assay
Summary page 2
…drug of abuse test result, particularly when the preliminary result is positive. 510k K111929 K011426 Measurand Carboxy-THC /Cannabinoids Carboxy-THC /Cannabinoids Matrix Human head or…
Psychemedics Corp.2002—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K122759Omega Laboratories Hair Drug Screening Assay Cardoxy-THC (Thca)Omega Laboratories, Inc.20120

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • Of its descendants, K122759 (Omega Laboratories, Inc., 2012) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LDJ devices

LDJ Enzyme Immunoassay, Cannabinoids: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · LDJ

2in 2024

2008: 22009: 12011: 42012: 42013: 32014: 22015: 32016: 12019: 12023: 12024: 2
2007high 4 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LDJ

48in 2015

2011: 219 days median2012: 193 days median2013: 162 days median2015: 48 days median
2007high 219 (2011) · low 48 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LDJ

1in 2023

2008: 42023: 1
2007high 4 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LDJ

1in 2015

2015: 1
2007high 1 (2015) · low 0 (2007)2025

MAUDE reports naming product code LDJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20082—40
20091—00
20100—00
2011421900
2012419300
2013316200
20142—00
201534801
20161—00
20170—00
20180—00
20191—00
20200—00
20210—00
20220—00
20231—10
20242—00
20250—00
20260—0—

What is it indicated for?

The Psychemedics Microplate EIA for Cannabinoids in Hair is an enzyme immunoassay (EIA) for the preliminary qualitative detection of cannabinoids in human head and body hair samples using a 11-nor-9-Carboxy- A9 -THC calibrator at 10 pg/10 mg hair cutoff for the purpose of identifying marijuana use. This is an in vitro diagnostic device intended exclusively for Psychemedics use only and is not intended for sale to anyone. The Psychemedics Chemiluminescent…

Read the full statement (131 words)

The Psychemedics Microplate EIA for Cannabinoids in Hair is an enzyme immunoassay (EIA) for the preliminary qualitative detection of cannabinoids in human head and body hair samples using a 11-nor-9-Carboxy- A9 -THC calibrator at 10 pg/10 mg hair cutoff for the purpose of identifying marijuana use. This is an in vitro diagnostic device intended exclusively for Psychemedics use only and is not intended for sale to anyone.

The Psychemedics Chemiluminescent Microplate EIA for Cannabinoids assay provides only a preliminary analytical test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. Gas Chromatography/Mass Spectrometry/Mass Spectrometry (GC/MS/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111929: Psychemedics Cannabinoids Eia.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111929

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026