510(k) Report

510(k) · Cleared

Cleared

LMD Cryptosporidium Antigen Detection

K955345510(k) TraditionalCleared Jun 7, 1996199-day reviewClass II21 CFR 866.3220

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

Lmd Laboratories · MHJ Cryptosporidium Spp.

Cleared on Jun 7, 1996 after a 199-day review. The FDA summary names no predicate by number. 1 later device descends from it.

Decided
Jun 7, 1996
Review
199 days
Class
Class II
Product code
MHJ
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared1995200020052010201520202025
  1. This deviceK955345 LMD Cryptosporidium Antigen DetectionLmd Laboratories · 1996
  2. Descendant · cites it directly · 0 of its ownK031059 Ivd Cryptosporidium Antigen Detection Assay, Model CP-96Ivd Research, Inc. · 2003

Most influential descendants

Showing 1 of 1 · See all
  • K031059Ivd Cryptosporidium Antigen Detection Assay, Model CP-96Ivd Research, Inc. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K955345LMD Cryptosporidium Antigen DetectionLmd Laboratories1996—
+1K031059Ivd Cryptosporidium Antigen Detection Assay, Model CP-96Ivd Research, Inc.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K955345, 1996–2003Source: 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 MHJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

The FDA summary names no predicate by number.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K031059Ivd Cryptosporidium Antigen Detection Assay, Model CP-96Ivd Research, Inc.20030

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?

  • Of its descendants, K031059 (Ivd Research, Inc., 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MHJ devices

MHJ Cryptosporidium Spp.: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MHJ

1in 2017

2013: 12017: 1
2007high 1 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MHJ

Too few MHJ 510(k)s in any year since 2007 to give a median.

Recalls per year · MHJ

No recall names MHJ since 2007.

Adverse event reports per year · MHJ

No MAUDE report names MHJ since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20131—00
20140—00
20150—00
20160—00
20171—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K955345: LMD Cryptosporidium Antigen Detection.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K955345

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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